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

Gene ID: 7451, updated on 13-May-2022

Summary

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

See VWFP1 in Genome Data Viewer
Location:
22q11.1
Annotation release Status Assembly Chr Location
110 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 poly(ADP-ribose) polymerase family member 4 pseudogene 3 Neighboring gene ankyrin repeat domain 62 pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 1665 Neighboring gene XK related 3

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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)