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    NPVF neuropeptide VF precursor [ Homo sapiens (human) ]

    Gene ID: 64111, updated on 10-Dec-2024

    Summary

    Official Symbol
    NPVFprovided by HGNC
    Official Full Name
    neuropeptide VF precursorprovided by HGNC
    Primary source
    HGNC:HGNC:13782
    See related
    Ensembl:ENSG00000105954 MIM:616984; AllianceGenome:HGNC:13782
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    RFRP; C7orf9
    Summary
    Enables neuropeptide activity. Involved in negative regulation of gonadotropin secretion and neuropeptide signaling pathway. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Dec 2024]
    Orthologs
    NEW
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    Genomic context

    See NPVF in Genome Data Viewer
    Location:
    7p15.3
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (25224570..25228486, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (25360013..25363930, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (25264189..25268105, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901603 Neighboring gene uncharacterized LOC105375191 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:25227953-25228454 Neighboring gene ribosomal protein L7a pseudogene 41 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:25283553-25284311 Neighboring gene Sharpr-MPRA regulatory region 9537 Neighboring gene small nucleolar RNA U3 Neighboring gene tRNA splicing endonuclease subunit 15 pseudogene 3

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    NOT enables neuropeptide activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables neuropeptide activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables signaling receptor binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Process Evidence Code Pubs
    involved_in negative regulation of gonadotropin secretion IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in negative regulation of gonadotropin secretion IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in neuropeptide signaling pathway IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in neuropeptide signaling pathway IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in neuropeptide signaling pathway NAS
    Non-traceable Author Statement
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in extracellular region IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    pro-FMRFamide-related neuropeptide VF
    Names
    FMRFamide-related peptide
    FMRFamide-related peptides
    RFamide-related peptide
    neuropeptide NPVF

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_022150.3NP_071433.3  pro-FMRFamide-related neuropeptide VF precursor

      See identical proteins and their annotated locations for NP_071433.3

      Status: VALIDATED

      Source sequence(s)
      AB040290, AF440392, BM714303
      Consensus CDS
      CCDS5395.1
      UniProtKB/Swiss-Prot
      A4D164, Q7LE27, Q96PI9, Q9HCQ7
      Related
      ENSP00000222674.2, ENST00000222674.2

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      25224570..25228486 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      25360013..25363930 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)