PRLHR (prolactin releasing hormone receptor)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 2834 |
| Gene name | Prolactin releasing hormone receptor |
| Gene symbol | PRLHR |
| Synonyms (NCBI Gene) |
GPR10GR3PrRPR
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| Chromosome | 10 |
| Chromosome location | 10q26.11 |
| Summary | PRLHR is a 7-transmembrane domain receptor for prolactin-releasing hormone (PRLH; MIM 602663) that is highly expressed in anterior pituitary (Ozawa et al., 2002 [PubMed 11923475]).[supplied by OMIM, Mar 2008] |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P49683 | ||||||||||
| Protein name | Prolactin-releasing peptide receptor (PrRP receptor) (PrRPR) (G-protein coupled receptor 10) (hGR3) | ||||||||||
| Protein function | Receptor for prolactin-releasing peptide (PrRP). Implicated in lactation, regulation of food intake and pain-signal processing. | ||||||||||
| PDB | 8ZPS , 8ZPT , 9K26 , 9K27 | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Only detected in the pituitary gland and in all cell types of pituitary adenomas. {ECO:0000269|PubMed:10498338, ECO:0000269|PubMed:11923475}. | ||||||||||
| Sequence |
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| Sequence length | 370 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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)
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