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 |
|
||||||
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.
|
||||||
Gene Ontology | |||||||
Molecular Function |
|
||||||
Biological Process |
|
||||||
Cellular Component |
|
||||||
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 | ||||||