U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination
    • Showing Current items.

    WIZP1 WIZ pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 645598, updated on 10-Dec-2024

    Summary

    Official Symbol
    WIZP1provided by HGNC
    Official Full Name
    WIZ pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:51696
    See related
    AllianceGenome:HGNC:51696
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See WIZP1 in Genome Data Viewer
    Location:
    11p14.3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (23404068..23406397)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (23527882..23530211)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (23425614..23427943)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 2718 Neighboring gene uncharacterized LOC124902646 Neighboring gene NANOG hESC enhancer GRCh37_chr11:22944198-22944709 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:23054822-23055322 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:23055323-23055823 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:23210858-23211394 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr11:23325332-23326531 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_20960 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr11:23380849-23382048 Neighboring gene programmed cell death 2 like pseudogene Neighboring gene microRNA 8054 Neighboring gene THAP domain containing 12 pseudogene 4

    Genomic regions, transcripts, and products

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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_021812.3 

      Range
      1..2330
      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_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      23404068..23406397
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      23527882..23530211
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)