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Search the entire catalog of SABiosciences products by gene name, key word, or RefSeq number. To learn more about all of these products, visit our Send an Email to Technical Support.

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  2. Use Gene Symbols, key words, or RefSeq Accession Numbers for your gene of interest to find the catalog numbers for the corresponding products. To learn how to get RefSeq Accession Numbers, click here.
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Species:
Gene Name, symbol, description:      RefSeq Number:   
All Product Lines
RT≤ Profilerô PCR Array Pathway-Focused qRT-PCR Based Expression Profiling
RT≤ qPCR Primer Assay Gene-Specific Primers for qRT-PCR, Genome-Wide Availability
Cignalô Pathway Reporter Assays Cell-Based Assays for Rapidly Analyzing Pathway Signaling Activity
miScript miRNA PCR Array miScript miRNA PCR Array
Multi-Analyte Profiler ELISArray Kits Analyze 12 Cytokines or Chemokines Simultaneously Using ELISA
Single Analyte ELISArray Kits High Performance ELISA with the Best Possible Antibodies
EpiTect Methyl II PCR Arrays Pathway-Focused PCR Based DNA Methylation Analysis
EpiTect Methyl II PCR Primer Assay PCR Assays for DNA Methylation Analysis, Genome-Wide Availability
SureSilencingô shRNA Gene-Specific Plasmid-Based RNA Interference, Genome-Wide Availability
EpiTect ChIP qPCR Arrays Pathway-Focused qPCR Based Histone Modifications Analysis
        
Search Result: 196 gene(s) found matching 'RET'
Gene Symbol: RET (Human)Other Aliases: CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1, PTC, RET-ELE1, RET51
Refseq IDs: NM_020630, NM_020975, ENST00000340058, ENST00000355710, ENST00000479913, ENST00000498820
Description: Ret proto-oncogene
This gene, a member of the cadherin superfamily, encodes one of the receptor tyrosine kinases, which are cell-surface molecules that transduce signals for cell growth and differentiation. This gene plays a crucial role in neural crest development, and it can undergo oncogenic activation in vivo and in vitro by cytogenetic rearrangement. Mutations in this gene are associated with the disorders multiple endocrine neoplasia, type IIA, multiple endocrine neoplasia, type IIB, Hirschsprung disease, and medullary thyroid carcinoma. Two transcript variants encoding different isoforms have been found for this gene.
Products:
 RT≤ Profilerô PCR Array4 products

Gene Symbol: DHRS7 (Human)Other Aliases: SDR34C1, retDSR4, retSDR4
Refseq IDs: NM_016029, XM_005267757, ENST00000216500, ENST00000536410, ENST00000553328, ENST00000553986, ENST00000554101, ENST00000555171, ENST00000556502, ENST00000557137, ENST00000557185, ENST00000557326, ENST00000557751
Description: Dehydrogenase/reductase (SDR family) member 7
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: DHX30 (Human)Other Aliases: DDX30, RETCOR
Refseq IDs: NM_014966, NM_138615, NR_075079, ENST00000348968, ENST00000395745, ENST00000415400, ENST00000441384, ENST00000445061, ENST00000446256, ENST00000457607, ENST00000461905, ENST00000470959, ENST00000471082, ENST00000472718, ENST00000474183, ENST00000476446, ENST00000492893
Description: DEAH (Asp-Glu-Ala-His) box polypeptide 30
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a member of this family. The encoded protein has 97% sequence identity with the mouse HELG protein. Alternative splicing of this gene generates 3 transcript variants.
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RETN (Human)Other Aliases: ADSF, FIZZ3, RETN1, RSTN, XCP1
Refseq IDs: NM_020415, NM_001193374
Description: Resistin
This gene belongs to the family defined by the mouse resistin-like genes. The characteristic feature of this family is the C-terminal stretch of 10 cys residues with identical spacing. The mouse homolog of this protein is secreted by adipocytes, and may be the hormone potentially linking obesity to type II diabetes.
Products:
 RT≤ Profilerô PCR Array6 products

Gene Symbol: RETNLB (Human)Other Aliases: FIZZ1, FIZZ2, HXCP2, RELM-beta, RELMb, RELMbeta, XCP2
Refseq IDs: NM_032579, ENST00000295755, ENST00000482939
Description: Resistin like beta
Products:
 RT≤ Profilerô PCR Array1 products

Gene Symbol: RetSat (Human)Other Aliases:
Refseq IDs: NM_017750, XM_005264384, ENST00000263854, ENST00000295802, ENST00000409984, ENST00000429806, ENST00000438611, ENST00000449375, ENST00000457495, ENST00000475624, ENST00000482694, ENST00000490291
Description: Retinol saturase (all-trans-retinol 13,14-reductase)
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: XPR1 (Human)Other Aliases: SYG1, X3
Refseq IDs: NM_004736, NM_001135669, ENST00000367589, ENST00000367590, ENST00000464817, ENST00000467345, ENST00000498177
Description: Xenotropic and polytropic retrovirus receptor 1
Products:
 RT≤ Profilerô PCR Array1 products

Gene Symbol: VSX2 (Human)Other Aliases: CHX10, HOX10, MCOP2, MCOPCB3, RET1
Refseq IDs: NM_182894
Description: Visual system homeobox 2
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: TXNDC5 (Human)Other Aliases: ENDOPDI, ERP46, HCC-2, PDIA15, STRF8, UNQ364
Refseq IDs: NM_030810, NM_001145549, XM_005249430, ENST00000379757, ENST00000460138, ENST00000469459, ENST00000473453, ENST00000475802, ENST00000539054
Description: Thioredoxin domain containing 5 (endoplasmic reticulum)
This gene encodes a protein-disulfide isomerase. Its expression is induced by hypoxia and its role may be to protect hypoxic cells from apoptosis. This gene can be co-transcribed with the upstream gene MU.
Products:
 RT≤ Profilerô PCR Array1 products

Gene Symbol: TXNDC12 (Human)Other Aliases: AG1, AGR1, ERP16, ERP18, ERP19, PDIA16, TLP19, hAG-1, hTLP19
Refseq IDs: NM_015913, NR_046405, NR_046406, XM_005270909, ENST00000371626, ENST00000469458, ENST00000471493, ENST00000472624, ENST00000610127
Description: Thioredoxin domain containing 12 (endoplasmic reticulum)
TXNDC12 belongs to the thioredoxin superfamily (see TXN; MIM 187700). Members of this superfamily possess a thioredoxin fold with a consensus active-site sequence (CxxC) and have roles in redox regulation, defense against oxidative stress, refolding of disulfide-containing proteins, and regulation of transcription factors (Liu et al., 2003).[supplied by OMIM]
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: STRA8 (Human)Other Aliases:
Refseq IDs: NM_182489
Description: Stimulated by retinoic acid gene 8 homolog (mouse)
Products:
 RT≤ Profilerô PCR Array1 products

Gene Symbol: STRA6 (Human)Other Aliases: MCOPCB8, MCOPS9
Refseq IDs: NM_022369, NM_001142617, NM_001142618, NM_001142619, NM_001142620, NM_001199040, NM_001199041, NM_001199042, XM_005254589, XM_005254590, XR_243122, ENST00000323940, ENST00000395105, ENST00000416286, ENST00000423167, ENST00000432245, ENST00000449139, ENST00000535552, ENST00000545137, ENST00000563965, ENST00000569936, ENST00000571341, ENST00000572785, ENST00000572975, ENST00000573214, ENST00000573391, ENST00000573456, ENST00000573724, ENST00000574278, ENST00000574439, ENST00000574570, ENST00000575272
Description: Stimulated by retinoic acid gene 6 homolog (mouse)
Products:
 RT≤ Profilerô PCR Array1 products

Gene Symbol: STRA13 (Human)Other Aliases: CENP-X, CENPX, D9, FAAP10, MHF2
Refseq IDs: NM_144998, NM_001271006, NM_001271007, XM_005256339, ENST00000306704, ENST00000392359, ENST00000577379, ENST00000579520, ENST00000580090, ENST00000580435, ENST00000583767, ENST00000584347, ENST00000584514, ENST00000584600, ENST00000585091
Description: Stimulated by retinoic acid 13 homolog (mouse)
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: SIL1 (Human)Other Aliases: BAP, MSS, ULG5
Refseq IDs: NM_022464, NM_001037633, ENST00000265195, ENST00000394817, ENST00000440765, ENST00000503732, ENST00000504666, ENST00000505353, ENST00000505830, ENST00000505945, ENST00000507002, ENST00000508639, ENST00000508744, ENST00000509400, ENST00000509534, ENST00000513453, ENST00000515008
Description: SIL1 homolog, endoplasmic reticulum chaperone (S. cerevisiae)
This gene encodes a resident endoplasmic reticulum (ER), N-linked glycoprotein with an N-terminal ER targeting sequence, 2 putative N-glycosylation sites, and a C-terminal ER retention signal. This protein functions as a nucleotide exchange factor for another unfolded protein response protein. Mutations in this gene have been associated with Marinesco-Sjogren syndrome. Alternate transcriptional splice variants have been characterized.
Products:
 RT≤ Profilerô PCR Array3 products

Gene Symbol: SERP2 (Human)Other Aliases: C13orf21, RP11-269C23.1, bA269C23.1
Refseq IDs: NM_001010897
Description: Stress-associated endoplasmic reticulum protein family member 2
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: SERP1 (Human)Other Aliases: RAMP4
Refseq IDs: NM_014445, ENST00000239944, ENST00000463647, ENST00000479209, ENST00000484608, ENST00000487153, ENST00000490945, ENST00000491195, ENST00000491660
Description: Stress-associated endoplasmic reticulum protein 1
Products:
 RT≤ Profilerô PCR Array3 products

Gene Symbol: SAG (Human)Other Aliases: RP47, S-AG
Refseq IDs: NM_000541, XM_005246099, XM_005246100, XM_005246101, ENST00000409110, ENST00000412969, ENST00000415974, ENST00000447536, ENST00000449594, ENST00000453143, ENST00000461532, ENST00000462487, ENST00000469222, ENST00000471884, ENST00000473771, ENST00000474206, ENST00000474220, ENST00000476500, ENST00000479450, ENST00000483231, ENST00000492629
Description: S-antigen; retina and pineal gland (arrestin)
Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. S-arrestin, also known as S-antigen, is a major soluble photoreceptor protein that is involved in desensitization of the photoactivated transduction cascade. It is expressed in the retina and the pineal gland and inhibits coupling of rhodopsin to transducin in vitro. Additionally, S-arrestin is highly antigenic, and is capable of inducing experimental autoimmune uveoretinitis. Mutations in this gene have been associated with Oguchi disease, a rare autosomal recessive form of night blindness.
Products:
 RT≤ Profilerô PCR Array1 products

Gene Symbol: RXRG (Human)Other Aliases: NR2B3, RXRC
Refseq IDs: NM_006917, NR_033824, NM_001256570, NM_001256571, ENST00000359842, ENST00000465764, ENST00000470566
Description: Retinoid X receptor, gamma
This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the antiproliferative effects of retinoic acid (RA). This receptor forms dimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene is expressed at significantly lower levels in non-small cell lung cancer cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Products:
 RT≤ Profilerô PCR Array3 products

Gene Symbol: RXRB (Human)Other Aliases: DAUDI6, H-2RIIBP, NR2B2, RCoR-1
Refseq IDs: NM_021976, NM_001270401, XM_005249278, XM_005249279, XM_005249280, XM_005272854, XM_005272855, XM_005272856, XM_005275007, XM_005275008, XM_005275009, XM_005275149, XM_005275150, XM_005275151, XM_005275276, XM_005275277, XM_005275278, XM_005275438, XM_005275439, XM_005275440, ENST00000374680, ENST00000374685, ENST00000413614, ENST00000481441, ENST00000483281, ENST00000483821, ENST00000544186
Description: Retinoid X receptor, beta
This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). This receptor forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. The gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. An alternatively spliced transcript variant has been described, but its full length sequence has not been determined.
Products:
 RT≤ Profilerô PCR Array5 products

Gene Symbol: RXRA (Human)Other Aliases: NR2B1
Refseq IDs: NM_002957, XM_005263408, XM_005263409, ENST00000356384, ENST00000481739, ENST00000484822, ENST00000540193
Description: Retinoid X receptor, alpha
Retinoid X receptors (RXRs) and retinoic acid receptors (RARs), are nuclear receptors that mediate the biological effects of retinoids by their involvement in retinoic acid-mediated gene activation. These receptors exert their action by binding, as homodimers or heterodimers, to specific sequences in the promoters of target genes and regulating their transcription. The protein encoded by this gene is a member of the steroid and thyroid hormone receptor superfamily of transcriptional regulators.
Products:
 RT≤ Profilerô PCR Array7 products

Gene Symbol: RTN4RL2 (Human)Other Aliases: NGRH1, NgR2
Refseq IDs: NM_178570, XM_005273973
Description: Reticulon 4 receptor-like 2
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTN4RL1 (Human)Other Aliases: NGRH2, NgR3
Refseq IDs: NM_178568
Description: Reticulon 4 receptor-like 1
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTN4R (Human)Other Aliases: NGR, NOGOR
Refseq IDs: NM_023004, ENST00000043402, ENST00000416372, ENST00000425986, ENST00000463936, ENST00000469601, ENST00000474642
Description: Reticulon 4 receptor
This gene encodes the receptor for reticulon 4, oligodendrocyte myelin glycoprotein and myelin-associated glycoprotein. This receptor mediates axonal growth inhibition and may play a role in regulating axonal regeneration and plasticity in the adult central nervous system.
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTN4IP1 (Human)Other Aliases: NIMP
Refseq IDs: NM_032730, XM_005267166, ENST00000369063, ENST00000493619, ENST00000498091, ENST00000539449
Description: Reticulon 4 interacting protein 1
The product of this gene is a novel mitochondrial protein that interacts with reticulon 4, which is a potent inhibitor of regeneration following spinal cord injury. The interaction of reticulon 4 with mitochondrial proteins may provide insight into the mechanisms for reticulon-induced inhibition of neurite growth.
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTN4 (Human)Other Aliases: 250, ASY, NI220, NOGO, NOGO-A, NOGOC, NSP, NSP-CL, Nbla00271, Nbla10545, Nogo-B, Nogo-C, RTN-X, RTN4-A, RTN4-B1, RTN4-B2, RTN4-C
Refseq IDs: NM_007008, NM_020532, NM_153828, NM_207520, NM_207521, XM_005264434, ENST00000317610, ENST00000337526, ENST00000354474, ENST00000357376, ENST00000357732, ENST00000394609, ENST00000394611, ENST00000402434, ENST00000404909, ENST00000405240, ENST00000427710, ENST00000438462, ENST00000461004, ENST00000485749, ENST00000486085, ENST00000491592
Description: Reticulon 4
This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. The product of this gene is a potent neurite outgrowth inhibitor which may also help block the regeneration of the central nervous system in higher vertebrates. Alternatively spliced transcript variants derived both from differential splicing and differential promoter usage and encoding different isoforms have been identified.
Products:
 RT≤ Profilerô PCR Array5 products

Gene Symbol: RTN3P1 (Human)Other Aliases: RTN3P1
Refseq IDs: ENST00000536295
Description: Reticulon 3 pseudogene 1 [Source:HGNC Symbol;Acc:19212]
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTN3 (Human)Other Aliases: ASYIP, HAP, NSPL2, NSPLII, RTN3-A1
Refseq IDs: NM_006054, NM_201428, NM_201430, NM_201429, NM_001265589, NM_001265590, NM_001265591, NR_049750, NR_049751, ENST00000338850, ENST00000339997, ENST00000341307, ENST00000354497, ENST00000356000, ENST00000377819, ENST00000536011, ENST00000537981, ENST00000538995, ENST00000540798, ENST00000542238, ENST00000543123, ENST00000543552, ENST00000545432
Description: Reticulon 3
The reticulons are a group of highly conserved genes with preferential expression in neuroendocrine tissues (see, e.g., RTN1; MIM 600865).[supplied by OMIM]
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTN2 (Human)Other Aliases: NSP2, NSPL1, NSPLI, SPG12
Refseq IDs: NM_005619, NM_206901, NM_206900, XR_243948, ENST00000245923, ENST00000344680, ENST00000430715, ENST00000587597, ENST00000588036, ENST00000589384, ENST00000589628, ENST00000590526, ENST00000590746, ENST00000591286, ENST00000591789, ENST00000592064, ENST00000593129, ENST00000593187
Description: Reticulon 2
This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. Alternatively spliced transcript variants encoding different isoforms have been identified.
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTN1 (Human)Other Aliases: NSP
Refseq IDs: NM_021136, NM_206852, NM_206857, NM_001243115, ENST00000267484, ENST00000342503, ENST00000395090, ENST00000432103, ENST00000474911, ENST00000481205, ENST00000490111, ENST00000557422
Description: Reticulon 1
This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. Alternatively spliced transcript variants encoding different isoforms have been identified. Multiple promoters rather than alternative splicing of internal exons seem to be involved in this diversity.
Products:
 RT≤ Profilerô PCR Array2 products

Gene Symbol: RTL1 (Human)Other Aliases: MART1, Mar1, PEG11
Refseq IDs: NM_001134888, XM_005267632
Description: Retrotransposon-like 1
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RTBDN (Human)Other Aliases:
Refseq IDs: NM_031429, NM_001080997, NM_001270440, NM_001270441, NM_001270442, NM_001270443, NM_001270444, NM_001270445, XM_005260089, XM_005260090
Description: Retbindin
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 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RS1 (Human)Other Aliases: RS, XLRS1
Refseq IDs: NM_000330, ENST00000379984, ENST00000476595
Description: Retinoschisin 1
Products:
 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RRH (Human)Other Aliases:
Refseq IDs: NM_006583
Description: Retinal pigment epithelium-derived rhodopsin homolog
Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. This gene belongs to the seven-exon subfamily of mammalian opsin genes that includes opsin 5 and retinal G protein coupled receptor.
Products:
 RT≤ Profilerô PCR Array1 products

Gene Symbol: RPGRIP1 (Human)Other Aliases: CORD13, LCA6, RGI1, RGRIP, RPGRIP, RPGRIP1d
Refseq IDs: NM_020366, XM_005267878, XM_005267879, XM_005267880, XM_005267881, XM_005267882, XM_005267883, XM_005267884, ENST00000206660, ENST00000307974, ENST00000382933, ENST00000400017, ENST00000553500, ENST00000553927, ENST00000554303, ENST00000554750, ENST00000555322, ENST00000555489, ENST00000555587, ENST00000556336, ENST00000557351, ENST00000557606, ENST00000557771
Description: Retinitis pigmentosa GTPase regulator interacting protein 1
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 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RPGR (Human)Other Aliases: COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15
Refseq IDs: NM_000328, NM_001034853, XM_005272633, XM_005272634, ENST00000309513, ENST00000318842, ENST00000338898, ENST00000339363, ENST00000342811, ENST00000378505, ENST00000464437, ENST00000470183, ENST00000474584, ENST00000476559, ENST00000482855, ENST00000494707, ENST00000494841
Description: Retinitis pigmentosa GTPase regulator
This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined.
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 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RPE65 (Human)Other Aliases: LCA2, RP20, mRPE65, rd12, sRPE65
Refseq IDs: NM_000329
Description: Retinal pigment epithelium-specific protein 65kDa
This gene encodes a protein which is located in the retinal pigment epithelium and is involved in the production of 11-cis retinal and in visual pigment regeneration. There are two forms of this protein, a soluble form called sRPE65, and a palmitoylated, membrane-bound form known as mRPE65. mRPE65 serves as the palmitoyl donor for lecithin retinol acyl transferase (LRAT), the enzyme that catalyzes the vitamin A to all trans retinol step of the chromophore regeneration process. Both mRPE65 and sRPE65 also serve as regulatory proteins, with the ratio and concentrations of these molecules playing a role in the inhibition of 11-cis retinal synthesis. Mutations in this gene have been associated with Leber congenital amaurosis type 2 (LCA2) and retinitis pigmentosa.
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 RT≤ Profilerô PCR Array1 products

Gene Symbol: RP9 (Human)Other Aliases: PAP-1
Refseq IDs: NM_203288, ENST00000297157, ENST00000448915, ENST00000474370, ENST00000492391
Description: Retinitis pigmentosa 9 (autosomal dominant)
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 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RP2 (Human)Other Aliases: DELXp11.3, NM23-H10, NME10, TBCCD2, XRP2
Refseq IDs: NM_006915
Description: Retinitis pigmentosa 2 (X-linked recessive)
The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death
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 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RP1L1 (Human)Other Aliases: DCDC4B
Refseq IDs: NM_178857, ENST00000329335, ENST00000382483
Description: Retinitis pigmentosa 1-like 1
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 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: RP1 (Human)Other Aliases: DCDC4A, ORP1
Refseq IDs: NM_006269, XM_005251278
Description: Retinitis pigmentosa 1 (autosomal dominant)
Initially named for its response to in vivo retinal oxygen levels (designated ORP1 for 'oxygen-regulated protein-1'), this gene was subsequently linked to autosomal dominant retinitis pigmentosa and was renamed RP1 for 'retinitis pigmentosa 1'. The data suggest that mutations in this gene cause dominant RP, and that the encoded protein has an important but unknown role in photoreceptor biology.
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 RT≤ Profilerô PCR ArrayInquire

Gene Symbol: ROM1 (Human)Other Aliases: ROM, ROSP1, RP7, TSPAN23
Refseq IDs: NM_000327, ENST00000278833, ENST00000525801, ENST00000525947, ENST00000529273, ENST00000534093
Description: Retinal outer segment membrane protein 1
This gene is a member of a photoreceptor-specific gene family and encodes an integral membrane protein found in the photoreceptor disk rim of the eye. This protein can form homodimers or can heterodimerize with another photoreceptor, retinal degeneration slow (RDS). It is essential for disk morphogenesis, and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa.
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Gene Symbol: RLBP1 (Human)Other Aliases: CRALBP
Refseq IDs: NM_000326, ENST00000268125, ENST00000563254, ENST00000564388, ENST00000567787
Description: Retinaldehyde binding protein 1
The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens.
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 RT≤ Profilerô PCR Array2 products

Gene Symbol: RGR (Human)Other Aliases: RP44
Refseq IDs: NM_002921, NM_001012720, NM_001012722, ENST00000358110, ENST00000359452, ENST00000372092, ENST00000469446, ENST00000478727, ENST00000479725, ENST00000483660, ENST00000483744, ENST00000483771, ENST00000497161
Description: Retinal G protein coupled receptor
This gene encodes a putative retinal G-protein coupled receptor. The gene is a member of the opsin subfamily of the 7 transmembrane, G-protein coupled receptor 1 family. Like other opsins which bind retinaldehyde, it contains a conserved lysine residue in the seventh transmembrane domain. The protein acts as a photoisomerase to catalyze the conversion of all-trans-retinal to 11-cis-retinal. The reverse isomerization occurs with rhodopsin in retinal photoreceptor cells. The protein is exclusively expressed in tissue adjacent to retinal photoreceptor cells, the retinal pigment epithelium and Mueller cells. This gene may be associated with autosomal recessive and autosomal dominant retinitis pigmentosa (arRP and adRP, respectively). Alternative splicing results in multiple transcript variants encoding different isoforms.
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 RT≤ Profilerô PCR Array1 products

Gene Symbol: RGP1 (Human)Other Aliases: KIAA0258
Refseq IDs: NM_001080496, ENST00000378078, ENST00000456972, ENST00000496906
Description: RGP1 retrograde golgi transport homolog (S. cerevisiae)
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Gene Symbol: RGAG4 (Human)Other Aliases: 6430402L03Rik, MAR5, MART5
Refseq IDs: NM_001024455
Description: Retrotransposon gag domain containing 4
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Gene Symbol: RGAG1 (Human)Other Aliases: MAR9, MART9
Refseq IDs: NM_020769, XM_005262173, XM_005262174
Description: Retrotransposon gag domain containing 1
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Gene Symbol: RFPL4B (Human)Other Aliases: RNF211, RP11-506B6.6
Refseq IDs: NM_001013734
Description: Ret finger protein-like 4B
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Gene Symbol: RFPL4AP7 (Human)Other Aliases: RFPL4AP7
Refseq IDs: ENST00000520120
Description: Ret finger protein-like 4A pseudogene 7 [Source:HGNC Symbol;Acc:45143]
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Gene Symbol: RFPL4AP5 (Human)Other Aliases: RFPL4AP5
Refseq IDs: ENST00000514977
Description: Ret finger protein-like 4A pseudogene 5 [Source:HGNC Symbol;Acc:45144]
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Gene Symbol: RFPL4AP3 (Human)Other Aliases: RFPL4AP3
Refseq IDs: ENST00000515267
Description: Ret finger protein-like 4A pseudogene 3 [Source:HGNC Symbol;Acc:45139]
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Gene Symbol: RFPL4AP1 (Human)Other Aliases: RFPL4AP1
Refseq IDs: ENST00000530883
Description: Ret finger protein-like 4A pseudogene 1 [Source:HGNC Symbol;Acc:45138]
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Gene Symbol: RFPL4AL1 (Human)Other Aliases:
Refseq IDs: NM_001277397
Description: Ret finger protein-like 4A-like 1
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Gene Symbol: RFPL4A (Human)Other Aliases: RFPL4, RNF210
Refseq IDs: NM_001145014
Description: Ret finger protein-like 4A
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Gene Symbol: RFPL3 (Human)Other Aliases:
Refseq IDs: NM_006604, NM_001098535
Description: Ret finger protein-like 3
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Gene Symbol: RFPL2 (Human)Other Aliases: RNF79
Refseq IDs: NM_006605, NM_001098527, NM_001159545, NM_001159546, XM_005261310, ENST00000248980, ENST00000248983, ENST00000400236, ENST00000400237, ENST00000489846
Description: Ret finger protein-like 2
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Gene Symbol: RFPL1 (Human)Other Aliases: RNF78
Refseq IDs: NM_021026
Description: Ret finger protein-like 1
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Gene Symbol: RER1 (Human)Other Aliases:
Refseq IDs: NM_007033, XM_005244712, XM_005244713, ENST00000306256, ENST00000378512, ENST00000378513, ENST00000378518, ENST00000443438, ENST00000462129, ENST00000488353, ENST00000493207, ENST00000605895
Description: RER1 retention in endoplasmic reticulum 1 homolog (S. cerevisiae)
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Gene Symbol: RELB (Human)Other Aliases: I-REL, IREL, REL-B
Refseq IDs: NM_006509, XM_005259127, XM_005259128, ENST00000221452, ENST00000505236, ENST00000509229, ENST00000509480, ENST00000510184, ENST00000540120, ENST00000589972
Description: V-rel reticuloendotheliosis viral oncogene homolog B
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 RT≤ Profilerô PCR Array7 products

Gene Symbol: RELA (Human)Other Aliases: NFKB3, p65
Refseq IDs: NM_021975, NM_001145138, NM_001243984, NM_001243985, XM_005274148, ENST00000308639, ENST00000406246, ENST00000525301, ENST00000525658, ENST00000525693, ENST00000525858, ENST00000526257, ENST00000526283, ENST00000526738, ENST00000527074, ENST00000527749, ENST00000527874, ENST00000527909, ENST00000529330, ENST00000529389, ENST00000531238, ENST00000531484, ENST00000532776, ENST00000532879, ENST00000532999, ENST00000533187, ENST00000533546, ENST00000534283, ENST00000534305, ENST00000534558
Description: V-rel reticuloendotheliosis viral oncogene homolog A (avian)
NFKB1 (MIM 164011) or NFKB2 (MIM 164012) is bound to REL (MIM 164910), RELA, or RELB (MIM 604758) to form the NFKB complex. The p50 (NFKB1)/p65 (RELA) heterodimer is the most abundant form of NFKB. The NFKB complex is inhibited by I-kappa-B proteins (NFKBIA, MIM 164008 or NFKBIB, MIM 604495), which inactivate NFKB by trapping it in the cytoplasm. Phosphorylation of serine residues on the I-kappa-B proteins by kinases (IKBKA, MIM 600664, or IKBKB, MIM 603258) marks them for destruction via the ubiquitination pathway, thereby allowing activation of the NFKB complex. Activated NFKB complex translocates into the nucleus and binds DNA at kappa-B-binding motifs such as 5-prime GGGRNNYYCC 3-prime or 5-prime HGGARNYYCC 3-prime (where H is A, C, or T; R is an A or G purine; and Y is a C or T pyrimidine).[supplied by OMIM]
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 RT≤ Profilerô PCR Array17 products

Gene Symbol: REL (Human)Other Aliases: C-Rel
Refseq IDs: NM_002908, XM_005264470, XM_005264471, XM_005264472
Description: V-rel reticuloendotheliosis viral oncogene homolog (avian)
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 RT≤ Profilerô PCR Array9 products

Gene Symbol: RDH8 (Human)Other Aliases: PRRDH, SDR28C2
Refseq IDs: NM_015725, ENST00000171214, ENST00000587782, ENST00000589570, ENST00000591589
Description: Retinol dehydrogenase 8 (all-trans)
All-trans-retinol dehydrogenase (RDH8) is a visual cycle enzyme that reduces all-trans-retinal to all-trans-retinol in the presence of NADPH (Rattner et al., 2000). It is a member of the short chain dehydrogenase/reductase family and is located in the outer segments of photoreceptors; hence it is also known as photoreceptor retinol dehydrogenase. It is important in the visual cycle by beginning the rhodopsin regeneration pathway by reducing all-trans-retinal, the product of bleached and hydrolysed rhodopsin (Rando, 2001). This is a rate-limiting step in the visual cycle (Saari et al., 1998).[supplied by OMIM]
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Gene Symbol: RDH5 (Human)Other Aliases: 9cRDH, HSD17B9, RDH1, SDR9C5
Refseq IDs: NM_002905, NM_001199771, ENST00000257895, ENST00000547072, ENST00000547301, ENST00000548082, ENST00000548123, ENST00000548486, ENST00000550608, ENST00000551444, ENST00000552930, ENST00000553160, ENST00000553187
Description: Retinol dehydrogenase 5 (11-cis/9-cis)
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Gene Symbol: RDH16 (Human)Other Aliases: RODH-4, SDR9C8
Refseq IDs: NM_003708, XM_005269205, ENST00000360752, ENST00000398138
Description: Retinol dehydrogenase 16 (all-trans)
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Gene Symbol: RDH14 (Human)Other Aliases: PAN2, SDR7C4
Refseq IDs: NM_020905, ENST00000381249, ENST00000468071
Description: Retinol dehydrogenase 14 (all-trans/9-cis/11-cis)
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Gene Symbol: RDH13 (Human)Other Aliases: SDR7C3
Refseq IDs: NM_138412, NM_001145971, NR_027381, NR_027382, XM_005258473, XM_005277060, XM_005277093, XM_005277129, XM_005277154, XM_005277176, XM_005277199, XM_005277238, XM_005277295, XM_005278247, ENST00000291892, ENST00000396247, ENST00000415061, ENST00000586331, ENST00000586945, ENST00000587026, ENST00000587046, ENST00000587373, ENST00000587721, ENST00000588306, ENST00000588941, ENST00000589197, ENST00000589305, ENST00000589605, ENST00000590349, ENST00000591023, ENST00000591603, ENST00000591868, ENST00000591960, ENST00000592423, ENST00000592573, ENST00000593134
Description: Retinol dehydrogenase 13 (all-trans/9-cis)
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Gene Symbol: RDH12 (Human)Other Aliases: LCA13, LCA3, RP53, SDR7C2
Refseq IDs: NM_152443, ENST00000267502, ENST00000539142, ENST00000547463, ENST00000551171, ENST00000552873
Description: Retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
Retinoids are indispensable light-sensitive elements of vision and also serve as essential modulators of cellular differentiation and proliferation in diverse cell types. RDH12 belongs to a family of dual-specificity retinol dehydrogenases that metabolize both all-trans- and cis-retinols (Haeseleer et al., 2002).[supplied by OMIM]
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Gene Symbol: RDH11 (Human)Other Aliases: ARSDR1, CGI82, HCBP12, MDT1, PSDR1, RALR1, SCALD, SDR7C1
Refseq IDs: NM_016026, NM_001252650, XM_005267732, ENST00000381346, ENST00000428130, ENST00000553384, ENST00000553578, ENST00000553816, ENST00000554035, ENST00000554731, ENST00000556692, ENST00000557273, ENST00000557331, ENST00000557726
Description: Retinol dehydrogenase 11 (all-trans/9-cis/11-cis)
RHD11, a member of the short-chain dehydrogenase/reductase (SDR) superfamily of oxidoreductases, is expressed at high levels in prostate epithelium, and its expression is regulated by androgens.[supplied by OMIM]
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Gene Symbol: RDH10 (Human)Other Aliases: SDR16C4
Refseq IDs: NM_172037, XM_005251172, ENST00000240285, ENST00000518870, ENST00000519380, ENST00000521013, ENST00000521928
Description: Retinol dehydrogenase 10 (all-trans)
RDH10 generates all-trans retinal from all-trans retinol and may plan an important role in the photic visual cycle. All-trans retinal is isomerized to 11-cis retinal by the retinal G protein-coupled receptor (RGR; MIM 600342) when the retinal pigment epithelium (RPE) is illuminated.[supplied by OMIM]
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 RT≤ Profilerô PCR Array1 products

Gene Symbol: RD3L (Human)Other Aliases: TDRD9-AS1, TDRD9AS1
Refseq IDs: NM_001257268
Description: Retinal degeneration 3-like
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Gene Symbol: RD3 (Human)Other Aliases: C1orf36, LCA12
Refseq IDs: NM_183059, NM_001164688, ENST00000367002, ENST00000484910
Description: Retinal degeneration 3
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Gene Symbol: RCN3 (Human)Other Aliases: RLP49
Refseq IDs: NM_020650, XM_005259089, ENST00000270645, ENST00000593483, ENST00000593644, ENST00000597801, ENST00000598833
Description: Reticulocalbin 3, EF-hand calcium binding domain
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Gene Symbol: RCN2 (Human)Other Aliases: E6BP, ERC-55, ERC55, TCBP49
Refseq IDs: NM_002902, NM_001271837, ENST00000320963, ENST00000394883, ENST00000394885, ENST00000557805, ENST00000558598, ENST00000560833
Description: Reticulocalbin 2, EF-hand calcium binding domain
Reticulocalbin 2 is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. The RCN2 gene maps to the same region as type 4 Bardet-Biedl syndrome (MIM:600374), suggesting a possible causative role for reticulocalbin 2 in the disorder.
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Gene Symbol: RCN1P2 (Human)Other Aliases: RCN1P2
Refseq IDs: ENST00000398357, ENST00000545120
Description: Reticulocalbin 1, EF-hand calcium binding domain pseudogene 2 [Source:HGNC Symbol;Acc:39204]
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Gene Symbol: RCN1P1 (Human)Other Aliases: RCN1P1
Refseq IDs: ENST00000400413
Description: Reticulocalbin 1, EF-hand calcium binding domain pseudogene 1 [Source:HGNC Symbol;Acc:39205]
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Gene Symbol: RCN1 (Human)Other Aliases: HEL-S-84, PIG20, RCAL, RCN
Refseq IDs: NM_002901, ENST00000054950, ENST00000506388, ENST00000527337, ENST00000528630, ENST00000530146, ENST00000530348, ENST00000531345, ENST00000532474, ENST00000532721, ENST00000532942, ENST00000533898
Description: Reticulocalbin 1, EF-hand calcium binding domain
Reticulocalbin 1 is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. High conservation of amino acid residues outside of these motifs, in comparison to mouse reticulocalbin, is consistent with a possible biochemical function besides that of calcium binding.
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Gene Symbol: RBP7 (Human)Other Aliases: CRBP4, CRBPIV
Refseq IDs: NM_052960
Description: Retinol binding protein 7, cellular
Due to its chemical instability and low solubility in aqueous solution, vitamin A requires cellular retinol-binding proteins (CRBPs), such as RBP7, for stability, internalization, intercellular transfer, homeostasis, and metabolism.[supplied by OMIM]
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Gene Symbol: RBP5 (Human)Other Aliases: CRBP-III, CRBP3, CRBPIII
Refseq IDs: NM_031491, ENST00000266560, ENST00000542370, ENST00000542784, ENST00000543045
Description: Retinol binding protein 5, cellular
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Gene Symbol: RBP4 (Human)Other Aliases: RDCCAS
Refseq IDs: NM_006744, XM_005270023
Description: Retinol binding protein 4, plasma
This protein belongs to the lipocalin family and is the specific carrier for retinol (vitamin A alcohol) in the blood. It delivers retinol from the liver stores to the peripheral tissues. In plasma, the RBP-retinol complex interacts with transthyretin which prevents its loss by filtration through the kidney glomeruli. A deficiency of vitamin A blocks secretion of the binding protein posttranslationally and results in defective delivery and supply to the epidermal cells.
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 RT≤ Profilerô PCR Array3 products

Gene Symbol: RBP3 (Human)Other Aliases: D10S64, D10S65, D10S66, IRBP, RBPI, RP66
Refseq IDs: NM_002900
Description: Retinol binding protein 3, interstitial
Interphotoreceptor retinol-binding protein is a large glycoprotein known to bind retinoids and found primarily in the interphotoreceptor matrix of the retina between the retinal pigment epithelium and the photoreceptor cells. It is thought to transport retinoids between the retinal pigment epithelium and the photoreceptors, a critical role in the visual process.The human IRBP gene is approximately 9.5 kbp in length and consists of four exons separated by three introns. The introns are 1.6-1.9 kbp long. The gene is transcribed by photoreceptor and retinoblastoma cells into an approximately 4.3-kilobase mRNA that is translated and processed into a glycosylated protein of 135,000 Da. The amino acid sequence of human IRBP can be divided into four contiguous homology domains with 33-38% identity, suggesting a series of gene duplication events. In the gene, the boundaries of these domains are not defined by exon-intron junctions, as might have been expected. The first three homology domains and part of the fourth are all encoded by the first large exon, which is 3,180 base pairs long. The remainder of the fourth domain is encoded in the last three exons, which are 191, 143, and approximately 740 base pairs long, respectively.
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Gene Symbol: RBP2 (Human)Other Aliases: CRABP-II, CRBP2, CRBPII, RBPC2
Refseq IDs: NM_004164, XM_005247693
Description: Retinol binding protein 2, cellular
RBP2 is an abundant protein present in the small intestinal epithelium. It is thought to participate in the uptake and/or intracellular metabolism of vitamin A. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. RBP2 may also modulate the supply of retinoic acid to the nuclei of endometrial cells during the menstrual cycle.
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 RT≤ Profilerô PCR Array2 products

Gene Symbol: RBP1 (Human)Other Aliases: CRABP-I, CRBP, CRBP1, CRBPI, RBPC
Refseq IDs: NM_002899, NM_001130992, NM_001130993, ENST00000232219, ENST00000474490, ENST00000483943, ENST00000487424, ENST00000492918
Description: Retinol binding protein 1, cellular
RBP1 is the carrier protein involved in the transport of retinol (vitamin A alcohol) from the liver storage site to peripheral tissue. Vitamin A is a fat-soluble vitamin necessary for growth, reproduction, differentiation of epithelial tissues, and vision. The gene harbors four exons encoding 24, 59, 33, and 16 amino acid residues respectively. The second intervening sequence alone occupies 19 kb of the 21 kb of the gene.
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 RT≤ Profilerô PCR Array2 products

Gene Symbol: RBL2 (Human)Other Aliases: P130, Rb2
Refseq IDs: NM_005611, XM_005256083, ENST00000262133, ENST00000379935, ENST00000544405, ENST00000544545, ENST00000561512, ENST00000562837, ENST00000562850, ENST00000564605, ENST00000567964
Description: Retinoblastoma-like 2 (p130)
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 RT≤ Profilerô PCR Array6 products

Gene Symbol: RBL1 (Human)Other Aliases: CP107, PRB1, p107
Refseq IDs: NM_002895, NM_183404
Description: Retinoblastoma-like 1 (p107)
The protein encoded by this gene is similar in sequence and possibly function to the product of the retinoblastoma 1 (RB1) gene. The RB1 gene product is a tumor suppressor protein that appears to be involved in cell cycle regulation, as it is phosphorylated in the S to M phase transition and is dephosphorylated in the G1 phase of the cell cycle. Both the RB1 protein and the product of this gene can form a complex with adenovirus E1A protein and SV40 large T-antigen, with the SV40 large T-antigen binding only to the unphosphorylated form of each protein. In addition, both proteins can inhibit the transcription of cell cycle genes containing E2F binding sites in their promoters. Due to the sequence and biochemical similarities with the RB1 protein, it is thought that the protein encoded by this gene may also be a tumor suppressor. Two transcript variants encoding different isoforms have been found for this gene.
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Gene Symbol: RBBP9 (Human)Other Aliases: BOG, RBBP10
Refseq IDs: NM_006606, XM_005260652, ENST00000337227, ENST00000491835, ENST00000493184
Description: Retinoblastoma binding protein 9
The protein encoded by this gene is a retinoblastoma binding protein that may play a role in the regulation of cell proliferation and differentiation. Two alternatively spliced transcript variants of this gene with identical predicted protein products have been reported, one of which is a nonsense-mediated decay candidate.
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Gene Symbol: RBBP8P1 (Human)Other Aliases: RBBP8P1
Refseq IDs: ENST00000449447
Description: Retinoblastoma binding protein 8 pseudogene 1 [Source:HGNC Symbol;Acc:39583]
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Gene Symbol: RBBP8 (Human)Other Aliases: COM1, CTIP, JWDS, RIM, SAE2, SCKL2
Refseq IDs: NM_002894, NM_203291, NM_203292, XM_005258325, XM_005258326, ENST00000327155, ENST00000360790, ENST00000399721, ENST00000399722, ENST00000399725, ENST00000577445, ENST00000577588, ENST00000579124, ENST00000580892, ENST00000581687, ENST00000581819, ENST00000582354, ENST00000583057, ENST00000583594, ENST00000583700, ENST00000585177
Description: Retinoblastoma binding protein 8
The protein encoded by this gene is a ubiquitously expressed nuclear protein. It is found among several proteins that bind directly to retinoblastoma protein, which regulates cell proliferation. This protein complexes with transcriptional co-repressor CTBP. It is also associated with BRCA1 and is thought to modulate the functions of BRCA1 in transcriptional regulation, DNA repair, and/or cell cycle checkpoint control. It is suggested that this gene may itself be a tumor suppressor acting in the same pathway as BRCA1. Three transcript variants encoding two different isoforms have been found for this gene. More transcript variants exist, but their full-length natures have not been determined.
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 RT≤ Profilerô PCR Array2 products

Gene Symbol: RBBP7 (Human)Other Aliases: RbAp46
Refseq IDs: NM_002893, NM_001198719, XM_005274572, ENST00000330735, ENST00000380084, ENST00000380087, ENST00000404022, ENST00000416035, ENST00000425696, ENST00000444437, ENST00000465244, ENST00000468092, ENST00000481586, ENST00000486166, ENST00000493145
Description: Retinoblastoma binding protein 7
This protein is a ubiquitously expressed nuclear protein and belongs to a highly conserved subfamily of WD-repeat proteins. It is found among several proteins that binds directly to retinoblastoma protein, which regulates cell proliferation. The encoded protein is found in many histone deacetylase complexes, including mSin3 co-repressor complex. It is also present in protein complexes involved in chromatin assembly. This protein can interact with BRCA1 tumor-suppressor gene and may have a role in the regulation of cell proliferation and differentiation.
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Gene Symbol: RBBP6 (Human)Other Aliases: MY038, P2P-R, PACT, RBQ-1, SNAMA
Refseq IDs: NM_018703, NM_006910, NM_032626, XM_005255461, XM_005255462, XM_005255463, ENST00000319715, ENST00000348022, ENST00000381039, ENST00000452655, ENST00000562430, ENST00000562683, ENST00000564314, ENST00000564726, ENST00000567686, ENST00000568015, ENST00000568316, ENST00000570185
Description: Retinoblastoma binding protein 6
The retinoblastoma tumor suppressor (pRB) protein binds with many other proteins. In various human cancers, pRB suppresses cellular proliferation and is inactivated. Cell cycle-dependent phosphorylation regulates the activity of pRB. This gene encodes a protein which binds to underphosphorylated but not phosphorylated pRB. Multiple alternatively spliced transcript variants that encode different isoforms have been found for this gene.
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 RT≤ Profilerô PCR Array1 products

Gene Symbol: RBBP5 (Human)Other Aliases: RBQ3, SWD1
Refseq IDs: NM_005057, NM_001193272, NM_001193273, XM_005245398, XM_005245399, XM_005245400, XM_005245401, XM_005245402, ENST00000264515, ENST00000367164, ENST00000484379
Description: Retinoblastoma binding protein 5
The protein encoded by this gene is a ubiquitously expressed nuclear protein and belongs to a highly conserved subfamily of WD-repeat proteins. It is found among several proteins that bind directly to retinoblastoma protein, which regulates cell proliferation. The encoded protein interacts preferentially with the underphosphorylated retinoblastoma protein via the E1A-binding pocket B.
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Gene Symbol: RBBP4P6 (Human)Other Aliases: RBBP4P6
Refseq IDs: ENST00000508098
Description: Retinoblastoma binding protein 4 pseudogene 6 [Source:HGNC Symbol;Acc:42373]
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Gene Symbol: RBBP4P5 (Human)Other Aliases: RBBP4P5
Refseq IDs: ENST00000398583
Description: Retinoblastoma binding protein 4 pseudogene 5 [Source:HGNC Symbol;Acc:42372]
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Gene Symbol: RBBP4P4 (Human)Other Aliases: RBBP4P4
Refseq IDs: ENST00000398588
Description: Retinoblastoma binding protein 4 pseudogene 4 [Source:HGNC Symbol;Acc:42371]
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Gene Symbol: RBBP4P3 (Human)Other Aliases: RBBP4P3
Refseq IDs: ENST00000399980
Description: Retinoblastoma binding protein 4 pseudogene 3 [Source:HGNC Symbol;Acc:42370]
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Gene Symbol: RBBP4P2 (Human)Other Aliases: RBBP4P2
Refseq IDs: ENST00000478252
Description: Retinoblastoma binding protein 4 pseudogene 2 [Source:HGNC Symbol;Acc:42369]
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Gene Symbol: RBBP4P1 (Human)Other Aliases: RBBP4P1
Refseq IDs: ENST00000502424
Description: Retinoblastoma binding protein 4 pseudogene 1 [Source:HGNC Symbol;Acc:42368]
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Gene Symbol: RBBP4 (Human)Other Aliases: NURF55, RBAP48
Refseq IDs: NM_005610, NM_001135255, NM_001135256, XM_005271093, ENST00000373485, ENST00000373493, ENST00000401893, ENST00000414241, ENST00000445722, ENST00000458695, ENST00000460669, ENST00000463378, ENST00000465780, ENST00000475321, ENST00000477563, ENST00000482190, ENST00000490500, ENST00000492348, ENST00000524393, ENST00000525506, ENST00000526193, ENST00000527118, ENST00000531983, ENST00000544435
Description: Retinoblastoma binding protein 4
This gene encodes a ubiquitously expressed nuclear protein which belongs to a highly conserved subfamily of WD-repeat proteins. It is present in protein complexes involved in histone acetylation and chromatin assembly. It is part of the Mi-2 complex which has been implicated in chromatin remodeling and transcriptional repression associated with histone deacetylation. This encoded protein is also part of co-repressor complexes, which is an integral component of transcriptional silencing. It is found among several cellular proteins that bind directly to retinoblastoma protein to regulate cell proliferation. This protein also seems to be involved in transcriptional repression of E2F-responsive genes.
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 RT≤ Profilerô PCR Array1 products

Gene Symbol: RB1 (Human)Other Aliases: OSRC, RB, p105-Rb, pRb, pp110
Refseq IDs: NM_000321, ENST00000267163, ENST00000467505, ENST00000480491, ENST00000484879, ENST00000525036, ENST00000531171
Description: Retinoblastoma 1
Retinoblastoma (RB) is an embryonic malignant neoplasm of retinal origin. It almost always presents in early childhood and is often bilateral. Spontaneous regression ('cure') occurs in some cases.[supplied by OMIM]
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 RT≤ Profilerô PCR Array21 products

Gene Symbol: RAX2 (Human)Other Aliases: ARMD6, CORD11, QRX, RAXL1
Refseq IDs: NM_032753, XM_005259662
Description: Retina and anterior neural fold homeobox 2
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Gene Symbol: RAX (Human)Other Aliases: MCOP3, RX
Refseq IDs: NM_013435, ENST00000256852, ENST00000334889, ENST00000555288, ENST00000591550
Description: Retina and anterior neural fold homeobox
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Gene Symbol: RARRES3 (Human)Other Aliases: 2-3, HRASLS4, HRSL4, PLA1, RIG1, TIG3
Refseq IDs: NM_004585, ENST00000255688, ENST00000354445, ENST00000439013, ENST00000537871, ENST00000544107
Description: Retinoic acid receptor responder (tazarotene induced) 3
Retinoids exert biologic effects such as potent growth inhibitory and cell differentiation activities and are used in the treatment of hyperproliferative dermatological diseases. These effects are mediated by specific nuclear receptor proteins that are members of the steroid and thyroid hormone receptor superfamily of transcriptional regulators. RARRES1, RARRES2, and RARRES3 are genes whose expression is upregulated by the synthetic retinoid tazarotene. RARRES3 is thought act as a tumor suppressor or growth regulator.
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Gene Symbol: RARRES2P9 (Human)Other Aliases: RARRES2P9
Refseq IDs: ENST00000565168
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 9 [Source:HGNC Symbol;Acc:48708]
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Gene Symbol: RARRES2P8 (Human)Other Aliases: RARRES2P8
Refseq IDs: ENST00000566335
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 8 [Source:HGNC Symbol;Acc:48707]
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Gene Symbol: RARRES2P7 (Human)Other Aliases: RARRES2P7
Refseq IDs: ENST00000567349
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 7 [Source:HGNC Symbol;Acc:48709]
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Gene Symbol: RARRES2P6 (Human)Other Aliases: RARRES2P6
Refseq IDs: ENST00000567333
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 6 [Source:HGNC Symbol;Acc:48705]
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Gene Symbol: RARRES2P5 (Human)Other Aliases: RARRES2P5
Refseq IDs: ENST00000564013
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 5 [Source:HGNC Symbol;Acc:48704]
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Gene Symbol: RARRES2P4 (Human)Other Aliases: RARRES2P4
Refseq IDs: ENST00000514074
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 4 [Source:HGNC Symbol;Acc:48703]
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Gene Symbol: RARRES2P3 (Human)Other Aliases: RARRES2P3
Refseq IDs: ENST00000457739
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 3 [Source:HGNC Symbol;Acc:48702]
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Gene Symbol: RARRES2P2 (Human)Other Aliases: RARRES2P2
Refseq IDs: ENST00000394842
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 2 [Source:HGNC Symbol;Acc:48701]
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Gene Symbol: RARRES2P1 (Human)Other Aliases: RARRES2P1
Refseq IDs: ENST00000474487
Description: Retinoic acid receptor responder (tazarotene induced) 2 pseudogene 1 [Source:HGNC Symbol;Acc:48700]
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Gene Symbol: RARRES2 (Human)Other Aliases: HP10433, TIG2
Refseq IDs: NM_002889, XM_005250032, XM_005250033, ENST00000223271, ENST00000466675, ENST00000467793, ENST00000478771, ENST00000482669
Description: Retinoic acid receptor responder (tazarotene induced) 2
Retinoids exert biologic effects such as potent growth inhibitory and cell differentiation activities and are used in the treatment of hyperproliferative dermatological diseases. These effects are mediated by specific nuclear receptor proteins that are members of the steroid and thyroid hormone receptor superfamily of transcriptional regulators. RARRES1, RARRES2, and RARRES3 are genes whose expression is upregulated by the synthetic retinoid tazarotene. RARRES2 is thought to act as a cell surface receptor.
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Gene Symbol: RARRES1 (Human)Other Aliases: LXNL, TIG1
Refseq IDs: NM_002888, NM_206963, XM_005247686, ENST00000237696, ENST00000462663, ENST00000471444, ENST00000479756, ENST00000498640
Description: Retinoic acid receptor responder (tazarotene induced) 1
This gene was identified as a retinoid acid (RA) receptor-responsive gene. It encodes a type 1 membrane protein. The expression of this gene is upregulated by tazarotene as well as by retinoic acid receptors. The expression of this gene is found to be downregulated in prostate cancer, which is caused by the methylation of its promoter and CpG island. Alternatively spliced transcript variant encoding distinct isoforms have been observed.
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Gene Symbol: RARG (Human)Other Aliases: NR1B3, RARC
Refseq IDs: NM_000966, NM_001042728, NM_001243730, NM_001243731, NM_001243732, XM_005269054, XM_005269055, XM_005269056, XM_005269057, ENST00000327550, ENST00000338561, ENST00000394426, ENST00000425354, ENST00000543726, ENST00000543762, ENST00000546377, ENST00000546717, ENST00000548284, ENST00000548317, ENST00000549859, ENST00000550265, ENST00000550350, ENST00000550362, ENST00000550721, ENST00000551158, ENST00000551501, ENST00000551580, ENST00000552901
Description: Retinoic acid receptor, gamma
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Gene Symbol: RARB (Human)Other Aliases: HAP, MCOPS12, NR1B2, RRB2
Refseq IDs: NM_000965, NM_016152, XM_005265361, XM_005265362, ENST00000330688, ENST00000383772, ENST00000404969, ENST00000437042, ENST00000458646, ENST00000462272, ENST00000479097, ENST00000480001, ENST00000489694
Description: Retinoic acid receptor, beta
This gene encodes retinoic acid receptor beta, a member of the thyroid-steroid hormone receptor superfamily of nuclear transcriptional regulators. This receptor localizes to the cytoplasm and to subnuclear compartments. It binds retinoic acid, the biologically active form of vitamin A which mediates cellular signalling in embryonic morphogenesis, cell growth and differentiation. It is thought that this protein limits growth of many cell types by regulating gene expression. The gene was first identified in a hepatocellular carcinoma where it flanks a hepatitis B virus integration site. The gene expresses at least two transcript variants; one additional transcript has been described, but its full length nature has not been determined.
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Gene Symbol: RARA (Human)Other Aliases: NR1B1, RAR
Refseq IDs: NM_000964, NM_001024809, NM_001145301, NM_001145302, XM_005257552, XM_005257553, XM_005257554, XM_005257555, XM_005257556, ENST00000254066, ENST00000394081, ENST00000394086, ENST00000394089, ENST00000420042, ENST00000425707, ENST00000475125, ENST00000577646, ENST00000579727, ENST00000582914
Description: Retinoic acid receptor, alpha
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Gene Symbol: RAI2 (Human)Other Aliases:
Refseq IDs: NM_021785, NM_001172732, NM_001172739, NM_001172743, NR_033348, NR_033349, ENST00000331511, ENST00000360011, ENST00000415486, ENST00000451717, ENST00000509491, ENST00000545871
Description: Retinoic acid induced 2
Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this intronless, retinoic acid-induced gene has not yet been determined; however, it has been suggested to play a role in development. Localization of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked mental retardation, oral-facial-digital syndrome, and Fried syndrome.
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Gene Symbol: RAI14 (Human)Other Aliases: NORPEG, RAI13
Refseq IDs: NM_015577, NM_001145520, NM_001145521, NM_001145522, NM_001145523, NM_001145525, XM_005248284, XM_005248285, XM_005248286, ENST00000265109, ENST00000397449, ENST00000428746, ENST00000502736, ENST00000503222, ENST00000503673, ENST00000504052, ENST00000505185, ENST00000506376, ENST00000507276, ENST00000507502, ENST00000507883, ENST00000508315, ENST00000508777, ENST00000509247, ENST00000510319, ENST00000510386, ENST00000511652, ENST00000512305, ENST00000512625, ENST00000512629, ENST00000513772, ENST00000513974, ENST00000514036, ENST00000514527, ENST00000514873, ENST00000514931, ENST00000515448, ENST00000515799
Description: Retinoic acid induced 14
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Gene Symbol: RAI1 (Human)Other Aliases: SMCR, SMS
Refseq IDs: NM_030665, ENST00000261641, ENST00000353383, ENST00000395774, ENST00000471135, ENST00000489697, ENST00000582514, ENST00000583166
Description: Retinoic acid induced 1
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients.
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Gene Symbol: RAET1M (Human)Other Aliases: RAET1M
Refseq IDs: ENST00000405282
Description: Retinoic acid early transcript 1M pseudogene [Source:HGNC Symbol;Acc:16799]
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Gene Symbol: RAET1L (Human)Other Aliases: ULBP6
Refseq IDs: NM_130900
Description: Retinoic acid early transcript 1L
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Gene Symbol: RAET1K (Human)Other Aliases: RAET1K
Refseq IDs: ENST00000403651, ENST00000533735, NR_024045
Description: Retinoic acid early transcript 1K pseudogene
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Gene Symbol: RAET1G (Human)Other Aliases: ULBP5
Refseq IDs: NM_001001788, XR_245515, ENST00000367360, ENST00000367361, ENST00000479265
Description: Retinoic acid early transcript 1G
Members of the RAET1 family, such as RAET1G, are major histocompatibility complex (MHC) class I-related genes located within a 180-kb cluster on chromosome 6q24.2-q25.3. RAET1 proteins contain MHC class I-like alpha-1 and alpha-2 domains. RAET1E (MIM 609243) and RAET1G differ from the other RAET1 proteins (e.g., RAET1I, or ULBP1; MIM 605697) in that they have type I membrane-spanning sequences at their C termini rather than glycosylphosphatidylinositol anchor sequences. (Radosavljevic et al., 2002).[supplied by OMIM]
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Gene Symbol: RAET1E (Human)Other Aliases: LETAL, N2DL-4, NKG2DL4, RAET1E2, RL-4, ULBP4, bA350J20.7
Refseq IDs: NM_139165, NM_001243325, NM_001243327, NM_001243328, XR_245506, ENST00000357183, ENST00000367363, ENST00000392270, ENST00000524905, ENST00000529948, ENST00000531073, ENST00000532335
Description: Retinoic acid early transcript 1E
Members of the RAET1 family, such as RAET1E, are major histocompatibility complex (MHC) class I-related genes located within a 180-kb cluster on chromosome 6q24.2-q25.3. RAET1 proteins contain MHC class I-like alpha-1 and alpha-2 domains. RAET1E and RAET1G (MIM 609244) differ from the other RAET1 proteins (e.g., RAET1I, or ULBP1; MIM 605697) in that they have type I membrane-spanning sequences at their C termini rather than glycosylphosphatidylinositol anchor sequences. (Radosavljevic et al., 2002).[supplied by OMIM]
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Gene Symbol: PRPH2 (Human)Other Aliases: AOFMD, AVMD, CACD2, DS, PRPH, RDS, RP7, TSPAN22, rd2
Refseq IDs: NM_000322, XM_005249261
Description: Peripherin 2 (retinal degeneration, slow)
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein found in the outer segment of both rod and cone photoreceptor cells. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. This protein is essential for disk morphogenesis. Defects in this gene are associated with both central and peripheral retinal degenerations. Some of the various phenotypically different disorders are autosomal dominant retinitis pigmentosa, progressive macular degeneration, macular dystrophy and retinitis pigmentosa digenic.
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Gene Symbol: P4HTM (Human)Other Aliases: EGLN4, HIFPH4, P4H-TM, PH-4, PH4, PHD4
Refseq IDs: NM_177939, NM_177938, XM_005265235, XR_245139, ENST00000343546, ENST00000383729, ENST00000444213, ENST00000468374, ENST00000472301, ENST00000472796, ENST00000475629, ENST00000484115, ENST00000485210, ENST00000486817, ENST00000491739, ENST00000609406
Description: Prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)
The product of this gene belongs to the family of prolyl 4-hydroxylases. This protein is a prolyl hydroxylase that may be involved in the degradation of hypoxia-inducible transcription factors under normoxia. It plays a role in adaptation to hypoxia and may be related to cellular oxygen sensing. Alternatively spliced variants encoding different isoforms have been identified.
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Gene Symbol: OS9 (Human)Other Aliases: ERLEC2, OS-9
Refseq IDs: NM_006812, NM_001017956, NM_001017957, NM_001017958, NM_001261420, NM_001261421, NM_001261422, NM_001261423, XM_005268581, XM_005268582, ENST00000257966, ENST00000315970, ENST00000389142, ENST00000389146, ENST00000413095, ENST00000435406, ENST00000439210, ENST00000546916, ENST00000547079, ENST00000549307, ENST00000549897, ENST00000550202, ENST00000550372, ENST00000550438, ENST00000550699, ENST00000550793, ENST00000550848, ENST00000551035, ENST00000551285, ENST00000552285, ENST00000552423, ENST00000552787, ENST00000553208
Description: Osteosarcoma amplified 9, endoplasmic reticulum lectin
This gene encodes a protein that is highly expressed in osteosarcomas. This protein binds to the hypoxia-inducible factor 1 (HIF-1), a key regulator of the hypoxic response and angiogenesis, and promotes the degradation of one of its subunits. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
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