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    VWA8P1 von Willebrand factor A domain containing 8 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 106480787, updated on 17-Sep-2024

    Summary

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    Official Symbol
    VWA8P1provided by HGNC
    Official Full Name
    von Willebrand factor A domain containing 8 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:44271
    See related
    Ensembl:ENSG00000250289 AllianceGenome:HGNC:44271
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

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    See VWA8P1 in Genome Data Viewer
    Location:
    5q13.1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (68854910..68855085, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (69677284..69677459, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (68150737..68150912, complement)

    Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379013 Neighboring gene uncharacterized LOC105379010 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr5:67975383-67976582 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22637 Neighboring gene uncharacterized LOC124900991 Neighboring gene U8 small nucleolar RNA Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr5:68194494-68195693 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:68217653-68218234 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:68218235-68218815 Neighboring gene uncharacterized LOC105379015

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    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)

    General gene information

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    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_044066.1 

      Range
      101..276
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      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_000005.10 Reference GRCh38.p14 Primary Assembly

      Range
      68854910..68855085 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060929.1 Alternate T2T-CHM13v2.0

      Range
      69677284..69677459 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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