C8orf37

Gene Information
  • Official Symbol: C8orf37
  • Official Name: chromosome 8 open reading frame 37
  • Aliases and Previous Symbols: N/A
  • Entrez ID: 157657
  • UniProt: Q96NL8
  • Interactions: BioGRID
  • PubMed articles: Open PubMed
  • OMIM: N/A
Function Summary
  • Entrez Summary: 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].
  • UniProt Summary: N/A

Pfam Domains GO Terms


CRISPR Data

Compound Hit Most Correlated Genes in Chemogenomics Tissues where Essential in the Avana Dataset (DepMap 20Q1)

Essentiality in NALM6
  • Essentiality Rank: 15046
  • Expression level (log2 read counts): 3.56

Expression Distribution

  • Last modified: 2025/12/10 20:19
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