C8orf37, chromosome 8 open reading frame 37

C8orf37, chromosome 8 open reading frame 37

• This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]

• Gene Synonyms (protein C8orf37, Bardet-Biedl syndrome 21, BBS21, CORD16, FAP418, MOT25, RP64, smalltalk,)
• NCBI Gene ID: 157657
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96NL8
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

chromosome 8 open reading frame 37 interacts with:

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.