1. Gene
  2. RRH - retinal pigment epithelium-derived rhodopsin homolog Gene

RRH - retinal pigment epithelium-derived rhodopsin homolog Gene

Homo sapiens
Gene ID: 10692 | Gene type: protein coding

About RRH

Cytogenetic location: 4q25 Genomic coordinates (GRCh38): 4:109,827,972-109,844,942 (from NCBI)

This gene has 3 transcripts (splice variants), 200 orthologues and 9 paralogues. Low expression observed in reference dataset.

Summary

Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. This gene belongs to the seven-exon subfamily of mammalian opsin genes that includes opsin 5 and retinal G protein coupled receptor. [provided by RefSeq, Jul 2008]

RRH Products(1)

mRNA Protein Name
NM_006583.5 NP_006574.1 visual pigment-like receptor peropsin
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

RRH Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (43 - 294)

  • 0
  • 100
  • 200
  • 300
  • 337 a.a.
Protein Preferred Names Protein Names

visual pigment-like receptor peropsin

peropsin

Related Diseases

Diseases Alias
Trombiculiasis
Subglottis Benign Neoplasm

Subglottic Tumor

Ulcerative Stomatitis

Stomatitis Ulcerative

Aphthous Stomatitis

Minor Oral Aphthous Ulceration

Noma

Cancrum Oris

Gangrenous Stomatitis

Oro-Facial Gangrene

Noma Neonatorum

Oral Gangrene

Oro-Facial Noma

Stomatitis Gangrenosa

Stomatonecrosis

Gangrene Stomatitis

Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1

Fundus Dystrophy

Retinal Dystrophy

Retinal Dystrophies

Dystrophy, Retinal

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta RRH VGNC VGNC:76940
Rattus norvegicus RRH RGD RGD:1308948
Felis catus RRH VGNC VGNC:64774
Canis familiaris RRH VGNC VGNC:45759
Bos taurus RRH VGNC VGNC:34163
Mus musculus RRH MGD MGI:1097709
Macaca fascicularis RRH NCBI NCBI:102119488
Others RRH NCBI