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MSH5


Official Full Name
mutS homolog 5
Organism
Homo sapiens
Gene ID
4439
Background
This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]
Synonyms
G7; NG23; POF13; MUTSH5; SPGF74

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Cat.No. Product Name Price
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MiUTR3H-05916 MSH5 miRNA 3'UTR clone Inquiry
CDCB186385 Rabbit MSH5 ORF clone (XM_008262597.1) Inquiry
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CDCL134591 Human Msh5 ORF clone (NM_001146215.1) Inquiry
CDCL138189 Human Ng23 ORF clone (NM_023893.4) Inquiry
CDCR252088 Mouse Msh5 ORF Clone(NM_013600.2) Inquiry
CDCR321265 Human MSH5 ORF Clone(NM_172165.3) Inquiry
CDCR368310 Rat Ng23 ORF Clone(NM_001004069.2) Inquiry
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