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
Not yet available
Cross-References
SwissProt Q96NL8
TrEMBL F4Y588
UniProt Splice Variant
Entrez Gene 157657
UniGene Hs.548157
RefSeq NM_177965
HUGO HGNC:27232
OMIM 614477
CCDS CCDS6268
HPRD
IMGT
EMBL AK055162 CH471060 GQ240139
GenPept ADE62519 BAB70866 EAW91744 EAW91745
RNA Seq Atlas 157657