NPVF (neuropeptide VF precursor)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 64111 |
| Gene name | Neuropeptide VF precursor |
| Gene symbol | NPVF |
| Synonyms (NCBI Gene) |
C7orf9RFRP
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| Chromosome | 7 |
| Chromosome location | 7p15.3 |
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miRNA
miRNA information provided by mirtarbase database.
57
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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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Q9HCQ7 | |
| Protein name | Pro-FMRFamide-related neuropeptide VF [Cleaved into: Neuropeptide NPSF; Neuropeptide RFRP-1; Neuropeptide RFRP-2; Neuropeptide NPVF (Neuropeptide RFRP-3)] | |
| Protein function | [Neuropeptide RFRP-1]: Efficiently inhibits forskolin-induced production of cAMP. Acts as a potent negative regulator of gonadotropin synthesis and secretion (PubMed:11025660, PubMed:20027225). Induces secretion of prolactin (By similarity). {EC | |
| Family and domains | ||
| Tissue specificity | TISSUE SPECIFICITY: [Isoform 1]: Specifically expressed in the retina. {ECO:0000269|PubMed:11951088}.; TISSUE SPECIFICITY: [Neuropeptide RFRP-1]: Detected in the hypothalamus. {ECO:0000269|PubMed:20027225}.; TISSUE SPECIFICITY: [Neuropeptide NPVF]: Detect | |
| Sequence |
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| Sequence length | 196 | |
| 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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