Homo sapiens Gene: C8orf37
Summary
InnateDB Gene IDBG-29319.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C8orf37
Gene Name chromosome 8 open reading frame 37
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000156172
Encoded Proteins
chromosome 8 open reading frame 37
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 8:95244919-95269201
Strand Reverse strand
Band q22.1
Transcripts
ENST00000286688 ENSP00000286688
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0007601 visual perception
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0030054 cell junction
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.548157
RefSeq NM_177965
HUGO
OMIM
CCDS CCDS6268
HPRD 14104
IMGT
EMBL
GenPept
RNA Seq Atlas