Bos taurus Gene: RHO | |||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Summary | |||||||||||||||||||||||||||||||
InnateDB Gene | IDBG-646351.3 | ||||||||||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||||||||||
Gene Symbol | RHO | ||||||||||||||||||||||||||||||
Gene Name | Rhodopsin | ||||||||||||||||||||||||||||||
Synonyms | |||||||||||||||||||||||||||||||
Species | Bos taurus | ||||||||||||||||||||||||||||||
Ensembl Gene | ENSBTAG00000001310 | ||||||||||||||||||||||||||||||
Encoded Proteins |
Rhodopsin
|
||||||||||||||||||||||||||||||
Protein Structure |
![]() |
||||||||||||||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||||||||||||||
Entrez Gene | |||||||||||||||||||||||||||||||
Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000163914:
Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25% of total cases, approximately 30% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq, Jul 2008] Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25%% of total cases, approximately 30%% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq, Jul 2008] |
||||||||||||||||||||||||||||||
Gene Information | |||||||||||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||||||||||
Genomic Location | Chromosome 22:56867887-56872817 | ||||||||||||||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||||||||||||||
Band | |||||||||||||||||||||||||||||||
Transcripts |
|
||||||||||||||||||||||||||||||
Interactions | |||||||||||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
They are also associated with 13 interaction(s) predicted by orthology.
|
||||||||||||||||||||||||||||||
Gene Ontology | |||||||||||||||||||||||||||||||
Molecular Function |
|
||||||||||||||||||||||||||||||
Biological Process |
|
||||||||||||||||||||||||||||||
Cellular Component |
|
||||||||||||||||||||||||||||||
Orthologs | |||||||||||||||||||||||||||||||
Species
Homo sapiens
Mus musculus
|
Gene ID
Gene Order
|
||||||||||||||||||||||||||||||
Pathways | |||||||||||||||||||||||||||||||
NETPATH | |||||||||||||||||||||||||||||||
REACTOME |
Signaling by GPCR pathway
The phototransduction cascade pathway
Opsins pathway
The canonical retinoid cycle in rods (twilight vision) pathway
Visual phototransduction pathway
G alpha (i) signalling events pathway
Activation of the phototransduction cascade pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
GPCR downstream signaling pathway
GPCR ligand binding pathway
Class A/1 (Rhodopsin-like receptors) pathway
Disease pathway
Inactivation, recovery and regulation of the phototransduction cascade pathway
|
||||||||||||||||||||||||||||||
KEGG | |||||||||||||||||||||||||||||||
INOH | |||||||||||||||||||||||||||||||
PID NCI | |||||||||||||||||||||||||||||||
Pathway Predictions based on Human Orthology Data | |||||||||||||||||||||||||||||||
NETPATH | |||||||||||||||||||||||||||||||
REACTOME |
G alpha (i) signalling events pathway
Opsins pathway
Class A/1 (Rhodopsin-like receptors) pathway
The canonical retinoid cycle in rods (twilight vision) pathway
Activation of the phototransduction cascade pathway
Signaling by GPCR pathway
Signal Transduction pathway
GPCR downstream signaling pathway
Diseases associated with visual transduction pathway
Visual phototransduction pathway
GPCR ligand binding pathway
The phototransduction cascade pathway
Inactivation, recovery and regulation of the phototransduction cascade pathway
Disease pathway
GPCR downstream signaling pathway
Disease pathway
Signaling by GPCR pathway
Class A/1 (Rhodopsin-like receptors) pathway
Opsins pathway
GPCR ligand binding pathway
G alpha (i) signalling events pathway
The canonical retinoid cycle in rods (twilight vision) pathway
Visual phototransduction pathway
Inactivation, recovery and regulation of the phototransduction cascade pathway
The phototransduction cascade pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Activation of the phototransduction cascade pathway
|
||||||||||||||||||||||||||||||
KEGG |
Phototransduction pathway
Phototransduction pathway
|
||||||||||||||||||||||||||||||
INOH | |||||||||||||||||||||||||||||||
PID NCI |
Visual signal transduction: Rods
|
||||||||||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||||||||||
SwissProt | P02699 | ||||||||||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||||||||||
Entrez Gene | 509933 | ||||||||||||||||||||||||||||||
UniGene | Bt.12753 | ||||||||||||||||||||||||||||||
RefSeq | NM_001014890 | ||||||||||||||||||||||||||||||
HUGO | |||||||||||||||||||||||||||||||
OMIM | |||||||||||||||||||||||||||||||
CCDS | |||||||||||||||||||||||||||||||
HPRD | |||||||||||||||||||||||||||||||
IMGT | |||||||||||||||||||||||||||||||
EMBL | K00502 K00503 K00504 K00505 K00506 M21606 | ||||||||||||||||||||||||||||||
GenPept | AAA30674 AAA30675 | ||||||||||||||||||||||||||||||
RNA Seq Atlas | 509933 | ||||||||||||||||||||||||||||||