Homo sapiens Gene: C2orf71
Summary
InnateDB Gene IDBG-41873.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C2orf71
Gene Name chromosome 2 open reading frame 71
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000179270
Encoded Proteins
chromosome 2 open reading frame 71
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa. [provided by RefSeq, Jun 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:29060976-29074261
Strand Reverse strand
Band p23.2
Transcripts
ENST00000331664 ENSP00000332809
ENST00000602958
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0007601 visual perception
GO:0050896 response to stimulus
Cellular Component
GO:0001750 photoreceptor outer segment
GO:0072372 primary cilium
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
RefSeq NM_001029883
HUGO
OMIM
CCDS CCDS42669
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas