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

Gene ID: 7451, updated on 10-Oct-2023

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_2023_10 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (16690097..16704461, complement)
105.20220307 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_2023_10

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

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