Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf116 gene product has been provisionally designated C1orf116 pending further characterization.
Function:
C1orf116 belongs to the SARG family. It is a putative androgen-specific receptor. It is highly expressed in prostate.
Subcellular Location:
Cytoplasmic
SWISS:
Q9BW04
Gene ID:
79098
Database links:
Entrez Gene: 79098 Human
Omim: 61336 Human
SwissProt: Q9BW04 Human
SwissProt: Q8BI29 Mouse
SwissProt: Q499V8 Rat
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