Expression of C8orf37 in cancer - Summary

CANCER ATLAS

Gene description

Chromosome 8 open reading frame 37

Protein class

Disease related genes, Predicted intracellular proteins

Protein evidence

Evidence at protein level

Colorectal cancer

Breast cancer

Prostate cancer

Lung cancer

Liver cancer

STAINING SUMMARY

HPA024198

GENE INFORMATION
Gene name	C8orf37 (HGNC Symbol)
Synonyms	CORD16, FLJ30600, RP64
Description	Chromosome 8 open reading frame 37 (HGNC Symbol)
Entrez gene 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]
Chromosome	8
Cytoband	q22.1
Chromosome location (bp)	95244919 - 95269201
Protein evidence	Evidence at protein level (all genes)
Ensembl	ENSG00000156172 (version 83.38)
Entrez gene	157657
UniProt	Q96NL8 (UniProt - Evidence at protein level)
neXtProt	NX_Q96NL8
Antibodypedia	C8orf37 antibodies

PROTEIN BROWSER

C8orf37-001

PROTEIN INFORMATION
Splice variant	UniProt	Protein class	Gene ontology	Length & mass	Signal peptide (predicted)	Transmembrane regions (predicted)
C8orf37-001 ENSP00000286688 ENST00000286688	Q96NL8 [Direct mapping] Protein C8orf37 F4Y588 [Target identity:100%; Query identity:100%] Chromosome 8 open reading frame 37, isoform CRA_a; Smalltalk Show all	Predicted intracellular proteins Disease related genes Protein evidence (Kim et al 2014) Protein evidence (Ezkurdia et al 2014) Show all	GO:0005737 [cytoplasm] GO:0005886 [plasma membrane] GO:0030054 [cell junction] Show all	207 aa 23.4 kDa	No	0