background:
Belonging to the UPF0690 family, C1orf52 is a 182 amino acid protein that is expressed in liver, heart, skeletal muscle, pancreas and kidney. There are three isoforms of C1orf52 that are produced as a result of alternative splicing events. The gene encoding C1orf52 maps to chromosome 1, 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.
Tissue Specificity:
Expressed in all tissues tested including heart, placenta, liver, skeletal muscle, kidney and pancreas. Weak expression in brain and lung.
Similarity:
Belongs to the UPF0690 family.
Database links:
Entrez Gene: 148423 Human
SwissProt: Q8N6N3 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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