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    VWFP1 von Willebrand factor pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 7451, updated on 17-Sep-2024

    Summary

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    Official Symbol
    VWFP1provided by HGNC
    Official Full Name
    von Willebrand factor pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:12727
    See related
    Ensembl:ENSG00000241717 AllianceGenome:HGNC:12727
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    VWFP; F8VWFL; F8VWFP
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    Genomic context

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    See VWFP1 in Genome Data Viewer
    Location:
    22q11.1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (16690097..16704461, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (17170987..17185351, complement)

    Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene ANKRD62P1-PARP4P3 readthrough, transcribed pseudogene Neighboring gene MPRA-validated peak4438 silencer Neighboring gene poly(ADP-ribose) polymerase family member 4 pseudogene 3 Neighboring gene ankyrin repeat domain 62 pseudogene 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr22:17177994-17178151 Neighboring gene MPRA-validated peak4439 silencer Neighboring gene long intergenic non-protein coding RNA 1665 Neighboring gene XK related 3

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Characterization and mapping of the 5' portion of von Willebrand factor pseudogene. Patracchini P, et al. Hum Genet, 1992 Nov. PMID 1487245
    2. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction. Mancuso DJ, et al. Biochemistry, 1991 Jan 8. PMID 1988024
    3. Phosphorylation of 69-kDa choline acetyltransferase at threonine 456 in response to amyloid-beta peptide 1-42. Dobransky T, et al. J Biol Chem, 2003 Feb 21. PMID 12486117

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    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.

    Genomic

    1. NG_001212.4 

      Range
      101..14465
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000022.11 Reference GRCh38.p14 Primary Assembly

      Range
      16690097..16704461 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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