With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf60 gene product has been provisionally designated C5orf60 pending further characterization.
Subcellular Location:
Membrane; Single-pass membrane protein (Potential).
SWISS:
A6NFR6
Gene ID:
285679
Database links:
Entrez Gene: 285679 Human
SwissProt: A6NFR6 Human
Unigene: 558748 Human
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