Gene Gene information from NCBI Gene database.
Entrez ID 64111
Gene name Neuropeptide VF precursor
Gene symbol NPVF
Synonyms (NCBI Gene)
C7orf9RFRP
Chromosome 7
Chromosome location 7p15.3
miRNA miRNA information provided by mirtarbase database.
57
miRTarBase ID miRNA Experiments Reference
MIRT715230 hsa-miR-4779 HITS-CLIP 19536157
MIRT715229 hsa-miR-3174 HITS-CLIP 19536157
MIRT715228 hsa-miR-885-5p HITS-CLIP 19536157
MIRT715227 hsa-miR-136-5p HITS-CLIP 19536157
MIRT715226 hsa-miR-6845-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0005102 Function Signaling receptor binding IBA
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IDA 11025660
GO:0007218 Process Neuropeptide signaling pathway IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616984 13782 ENSG00000105954
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
MEIISSKLFILLTLATSSLLTSNIFCADELVISNLHSKENYDKYSEPRGYPKGERSLNFE
ELKDWGPKNVIKMSTPAVNKMPHSFANLPLRFGRNVQEERSAGATANLPLRSGRNMEVSL
VRRVPNLPQRFGRTTTAKSVCRMLSDLCQGSMHSPCANDLFYSMTCQHQEIQNPDQKQSR
RLLFKKIDDAELKQEK
Sequence length 196
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Neuroactive ligand-receptor interaction  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
SCHIZOPHRENIA 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
Choroid Plexus Papilloma Choroid Plexus Papilloma BEFREE 25180599
★☆☆☆☆
Found in Text Mining only
Hyperglycemia Hyperglycemia BEFREE 30081043
★☆☆☆☆
Found in Text Mining only
Macular Edema, Cystoid Cystoid macular edema BEFREE 11951088
★☆☆☆☆
Found in Text Mining only
Obesity Obesity BEFREE 30075164
★☆☆☆☆
Found in Text Mining only