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Browse Products By Gene


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.

  1. Choose your species of interest first: Human, Mouse, Rat, Rhesus Macaque or Fruit Fly.
  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.
  3. Select the Product Line(s) that you would like to search.
  4. Click 'Submit'.
Species:
Gene Name, symbol, description:      RefSeq Number:   
All Product Lines
RT˛ Profiler™ PCR Array Pathway-Focused qRT-PCR Based Expression Profiling
RT˛ qPCR Primer Assay Gene-Specific Primers for qRT-PCR, Genome-Wide Availability
Cignal™ 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
SureSilencing™ shRNA Gene-Specific Plasmid-Based RNA Interference, Genome-Wide Availability
EpiTect ChIP qPCR Arrays Pathway-Focused qPCR Based Histone Modifications Analysis
        
Search Result: 40 gene(s) found matching 'MUT'
Gene Symbol: MUT (Human)Other Aliases: MCM
Refseq IDs: NM_000255, XM_005249143
Description: Methylmalonyl CoA mutase
MUT encodes the mitochondrial enzymne methylmalonyl Coenzyme A mutase. In humans, MUT is a vitamin B12-dependent enzyme which catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA, while in other species this enzyme may have different functions. Mutations in MUT may lead to various types of methylmalonic aciduria.
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Gene Symbol: EXD3 (Human)Other Aliases: mut-7
Refseq IDs: NM_017820, NM_001286823, NR_104598, NR_104599, XM_005266091, XM_005266092, XM_005266093
Description: Exonuclease 3'-5' domain containing 3
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Gene Symbol: MSH5 (Human)Other Aliases: G7, MUTSH5, NG23
Refseq IDs: NM_002441, NM_025259, NM_172166, NM_172165
Description: MutS homolog 5 (E. coli)
This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair or meiotic recombination processes. This protein is similar to a Saccharomyces cerevisiae protein that participates in meiotic segregation fidelity and crossing-over. This protein forms heterooligomers with another member of this family, mutS homolog 4. Alternative splicing results in four transcript variants encoding three different isoforms.
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Gene Symbol: MUTYH (Human)Other Aliases: CYP2C, MYH
Refseq IDs: NM_012222, NM_001048171, NM_001048172, NM_001048173, NM_001048174, NM_001128425, XM_005270880, XM_005270881, XM_005270882, XM_005270883, XM_005270884, XM_005270885, XM_005270886
Description: MutY homolog (E. coli)
This gene encodes a DNA glycosylase involved in oxidative DNA damage repair. The enzyme excises adenine bases from the DNA backbone at sites where adenine is inappropriately paired with guanine, cytosine, or 8-oxo-7,8-dihydroguanine, a major oxidatively damaged DNA lesion. The protein is localized to the nucleus and mitochondria. Mutations in this gene result in heritable predisposition to colon and stomach cancer. Multiple transcript variants encoding different isoforms have been found for this gene.
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Gene Symbol: SACM1L (Human)Other Aliases: SAC1
Refseq IDs: NM_014016, XM_005264965, XR_245103
Description: SAC1 suppressor of actin mutations 1-like (yeast)
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Gene Symbol: PGAM5P1 (Human)Other Aliases: PGAM5P1
Refseq IDs: ENST00000518923
Description: Phosphoglycerate mutase family member 5 pseudogene 1 [Source:HGNC Symbol;Acc:42467]
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Gene Symbol: PGAM5 (Human)Other Aliases: BXLBV68
Refseq IDs: NM_138575, NM_001170543, NM_001170544
Description: Phosphoglycerate mutase family member 5
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Gene Symbol: PGAM4P2 (Human)Other Aliases: PGAM4P2
Refseq IDs: ENST00000512491
Description: Phosphoglycerate mutase family member 4 pseudogene 2 [Source:HGNC Symbol;Acc:42466]
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Gene Symbol: PGAM4P1 (Human)Other Aliases: PGAM4P1
Refseq IDs: ENST00000426407
Description: Phosphoglycerate mutase family member 4 pseudogene 1 [Source:HGNC Symbol;Acc:42465]
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Gene Symbol: PGAM4 (Human)Other Aliases: PGAM-B, PGAM1, PGAM3, dJ1000K24.1
Refseq IDs: NM_001029891
Description: Phosphoglycerate mutase family member 4
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Gene Symbol: PGAM3P (Human)Other Aliases: PGAM3P
Refseq IDs: ENST00000437662
Description: Phosphoglycerate mutase 3, pseudogene [Source:HGNC Symbol;Acc:16557]
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Gene Symbol: PGAM2 (Human)Other Aliases: GSD10, PGAM-M, PGAMM
Refseq IDs: NM_000290
Description: Phosphoglycerate mutase 2 (muscle)
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Gene Symbol: PGAM1P9 (Human)Other Aliases: PGAM1P9
Refseq IDs: ENST00000503887
Description: Phosphoglycerate mutase 1 pseudogene 9 [Source:HGNC Symbol;Acc:42456]
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Gene Symbol: PGAM1P8 (Human)Other Aliases: PGAM1P8
Refseq IDs: ENST00000505544
Description: Phosphoglycerate mutase 1 pseudogene 8 [Source:HGNC Symbol;Acc:42455]
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Gene Symbol: PGAM1P7 (Human)Other Aliases: PGAM1P7
Refseq IDs: ENST00000413837
Description: Phosphoglycerate mutase 1 pseudogene 7 [Source:HGNC Symbol;Acc:42454]
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Gene Symbol: PGAM1P6 (Human)Other Aliases: PGAM1P6
Refseq IDs: ENST00000425684
Description: Phosphoglycerate mutase 1 pseudogene 6 [Source:HGNC Symbol;Acc:42453]
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Gene Symbol: PGAM1P4 (Human)Other Aliases: PGAM1P4
Refseq IDs: ENST00000334645, ENST00000397343
Description: Phosphoglycerate mutase 1 pseudogene 4 [Source:HGNC Symbol;Acc:42451]
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Gene Symbol: PGAM1P3 (Human)Other Aliases: PGAM1P3
Refseq IDs: ENST00000420790
Description: Phosphoglycerate mutase 1 pseudogene 3 [Source:HGNC Symbol;Acc:42450]
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Gene Symbol: PGAM1P2 (Human)Other Aliases: PGAM1P2
Refseq IDs: ENST00000436071
Description: Phosphoglycerate mutase 1 pseudogene 2 [Source:HGNC Symbol;Acc:42449]
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Gene Symbol: PGAM1P13 (Human)Other Aliases: PGAM1P13
Refseq IDs: ENST00000507497
Description: Phosphoglycerate mutase 1 pseudogene 13 [Source:HGNC Symbol;Acc:42461]
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Gene Symbol: PGAM1P12 (Human)Other Aliases: PGAM1P12
Refseq IDs: ENST00000505622
Description: Phosphoglycerate mutase 1 pseudogene 12 [Source:HGNC Symbol;Acc:42459]
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Gene Symbol: PGAM1P11 (Human)Other Aliases: PGAM1P11
Refseq IDs: ENST00000416729
Description: Phosphoglycerate mutase 1 pseudogene 11 [Source:HGNC Symbol;Acc:42464]
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Gene Symbol: PGAM1P10 (Human)Other Aliases: PGAM1P10
Refseq IDs: ENST00000402426
Description: Phosphoglycerate mutase 1 pseudogene 10 [Source:HGNC Symbol;Acc:42457]
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Gene Symbol: PGAM1P1 (Human)Other Aliases: PGAM1P1
Refseq IDs: ENST00000504014
Description: Phosphoglycerate mutase 1 pseudogene 1 [Source:HGNC Symbol;Acc:42448]
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Gene Symbol: PGAM1 (Human)Other Aliases: HEL-S-35, PGAM-B, PGAMA
Refseq IDs: NM_002629, XM_005269900
Description: Phosphoglycerate mutase 1 (brain)
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Gene Symbol: OGG1 (Human)Other Aliases: HMMH, HOGG1, MUTM, OGH1
Refseq IDs: NM_002542, NM_016819, NM_016820, NM_016821, NM_016826, NM_016827, NM_016828, NM_016829, XM_005265185
Description: 8-oxoguanine DNA glycosylase
This gene encodes the enzyme responsible for the excision of 8-oxoguanine, a mutagenic base byproduct which occurs as a result of exposure to reactive oxygen. The action of this enzyme includes lyase activity for chain cleavage. Alternative splicing of the C-terminal region of this gene classifies splice variants into two major groups, type 1 and type 2, depending on the last exon of the sequence. Type 1 alternative splice variants end with exon 7 and type 2 end with exon 8. All variants share the N-terminal region in common. Many alternative splice variants for this gene have been described, but the full-length nature for every variant has not been determined. The N-terminus of this gene contains a mitochondrial targetting signal, essential for mitochondrial localization.
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Gene Symbol: MUM1L1 (Human)Other Aliases:
Refseq IDs: NM_152423, NM_001171020, XM_005262076, XM_005262077, XM_005262078
Description: Melanoma associated antigen (mutated) 1-like 1
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Gene Symbol: MUM1 (Human)Other Aliases: EXPAND1, HSPC211, MUM-1
Refseq IDs: NM_032853, NR_024247
Description: Melanoma associated antigen (mutated) 1
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Gene Symbol: MSH6 (Human)Other Aliases: GTBP, GTMBP, HNPCC5, HSAP, p160
Refseq IDs: NM_000179, NM_001281492, NM_001281493, NM_001281494, XM_005264271
Description: MutS homolog 6 (E. coli)
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Gene Symbol: MSH4 (Human)Other Aliases:
Refseq IDs: NM_002440, XM_005270878
Description: MutS homolog 4 (E. coli)
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Gene Symbol: MSH3 (Human)Other Aliases: DUP, MRP1
Refseq IDs: NM_002439
Description: MutS homolog 3 (E. coli)
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Gene Symbol: MSH2 (Human)Other Aliases: COCA1, FCC1, HNPCC, HNPCC1, LCFS2
Refseq IDs: NM_000251, NM_001258281, XM_005264332, XM_005264333
Description: MutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
MSH2 was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC.
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Gene Symbol: MLH3 (Human)Other Aliases: HNPCC7
Refseq IDs: NM_014381, NM_001040108, XM_005267531, XM_005267532, XM_005267533, XM_005267534, XR_245681
Description: MutL homolog 3 (E. coli)
This gene is a member of the MutL-homolog (MLH) family of DNA mismatch repair (MMR) genes. MLH genes are implicated in maintaining genomic integrity during DNA replication and after meiotic recombination. The protein encoded by this gene functions as a heterodimer with other family members. Somatic mutations in this gene frequently occur in tumors exhibiting microsatellite instability, and germline mutations have been linked to hereditary nonpolyposis colorectal cancer type 7 (HNPCC7). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined.
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Gene Symbol: MLH1 (Human)Other Aliases: COCA2, FCC2, HNPCC, HNPCC2, hMLH1
Refseq IDs: NM_000249, NM_001167617, NM_001167618, NM_001167619, NM_001258271, NM_001258273, NM_001258274, XM_005265161, XM_005265162, XM_005265163, XM_005265164, XM_005265165, XM_005265166
Description: MutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)
This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). It is a human homolog of the E. coli DNA mismatch repair gene mutL, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Alternatively spliced transcript variants encoding different isoforms have been described, but their full-length natures have not been determined.
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Gene Symbol: MCC (Human)Other Aliases: MCC1
Refseq IDs: NM_002387, NM_001085377, XM_005271991, XM_005271992
Description: Mutated in colorectal cancers
MCC is a candidate for the putative colorectal tumor suppressor gene. The MCC gene product may be involved in early stages of colorectal neoplasia in both sporadic and familial tumors
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Gene Symbol: LOC100289673 (Human)Other Aliases:
Refseq IDs: NR_033175
Description: Phosphoglycerate mutase family member 5 pseudogene
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Gene Symbol: GALM (Human)Other Aliases: HEL-S-63p, IBD1
Refseq IDs: NM_138801, XR_244925
Description: Galactose mutarotase (aldose 1-epimerase)
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Gene Symbol: BPGM (Human)Other Aliases: DPGM
Refseq IDs: NM_001724, NM_199186, XM_005250545
Description: 2,3-bisphosphoglycerate mutase
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Gene Symbol: BLOC1S5 (Human)Other Aliases: BLOS5, MU, MUTED
Refseq IDs: NM_001199322, NM_001199323, NM_201280
Description: Muted homolog (mouse)
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Gene Symbol: ATM (Human)Other Aliases: AT1, ATA, ATC, ATD, ATDC, ATE, TEL1, TELO1
Refseq IDs: NM_000051, XM_005271561, XM_005271562, XM_005271563, XM_005271564
Description: Ataxia telangiectasia mutated
The protein encoded by this gene belongs to the PI3/PI4-kinase family. This protein is an important cell cycle checkpoint kinase that phosphorylates; thus, it functions as a regulator of a wide variety of downstream proteins, including tumor suppressor proteins p53 and BRCA1, checkpoint kinase CHK2, checkpoint proteins RAD17 and RAD9, and DNA repair protein NBS1. This protein and the closely related kinase ATR are thought to be master controllers of cell cycle checkpoint signaling pathways that are required for cell response to DNA damage and for genome stability. Mutations in this gene are associated with ataxia telangiectasia, an autosomal recessive disorder. Two transcript variants encoding different isoforms have been found for this gene.
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