Gene Gene information from NCBI Gene database.
Entrez ID 221391
Gene name Opsin 5
Gene symbol OPN5
Synonyms (NCBI Gene)
GPR136GRP136PGR12TMEM13
Chromosome 6
Chromosome location 6p12.3
Summary Opsins are members of the guanine nucleotide-binding protein (G protein)-coupled receptor superfamily. This opsin gene is expressed in the eye, brain, testes, and spinal cord. This gene belongs to the seven-exon subfamily of mammalian opsin genes that inc
miRNA miRNA information provided by mirtarbase database.
135
miRTarBase ID miRNA Experiments Reference
MIRT550747 hsa-miR-1277-5p PAR-CLIP 21572407
MIRT550745 hsa-miR-8485 PAR-CLIP 21572407
MIRT550746 hsa-miR-329-3p PAR-CLIP 21572407
MIRT550744 hsa-miR-362-3p PAR-CLIP 21572407
MIRT550743 hsa-miR-603 PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0001750 Component Photoreceptor outer segment IBA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005502 Function 11-cis retinal binding IEA
GO:0005502 Function 11-cis retinal binding IMP 22043319
GO:0005737 Component Cytoplasm IDA 30168605
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609042 19992 ENSG00000124818
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6U736
Protein name Opsin-5 (G-protein coupled receptor 136) (G-protein coupled receptor PGR12) (Neuropsin) (Transmembrane protein 13)
Protein function G-protein coupled receptor which selectively activates G(i) type G proteins via ultraviolet A (UVA) light-mediated activation in the retina (By similarity). Preferentially binds the chromophore 11-cis retinal and is a bistable protein that displ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 50 306 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain and retina and cell lines derived from neural retina. {ECO:0000269|PubMed:14623103}.
Sequence
Sequence length 354
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    G alpha (i) signalling events
Opsins
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
NEPHROTIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PERIPHERAL ARTERIAL DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Bipolar Disorder Bipolar Disorder BEFREE 18354391
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Bipolar Disorder LHGDN 18354391
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 16614108
★☆☆☆☆
Found in Text Mining only
Carcinoma, Ovarian Epithelial Ovarian Epithelial carcinoma BEFREE 11309326
★☆☆☆☆
Found in Text Mining only
Cerebral Infarction Cerebral Infarction BEFREE 15082799
★☆☆☆☆
Found in Text Mining only
Depressive disorder Mental Depression BEFREE 28267150, 28636578, 31477683
★☆☆☆☆
Found in Text Mining only
Depressive Disorder Major depressive disorder Pubtator 31477683, 34715912 Associate
★☆☆☆☆
Found in Text Mining only
Dermatitis Dermatitis BEFREE 20500798
★☆☆☆☆
Found in Text Mining only
Epilepsy, Temporal Lobe Epilepsy BEFREE 28267150
★☆☆☆☆
Found in Text Mining only
Hyperkeratosis Hyperkeratosis BEFREE 20500798
★☆☆☆☆
Found in Text Mining only