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    WEE2P1 WEE2 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 100420018, updated on 10-Oct-2023

    Summary

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    Official Symbol
    WEE2P1provided by HGNC
    Official Full Name
    WEE2 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:51823
    See related
    Ensembl:ENSG00000254672
    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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    Location:
    11p13
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (35966810..35968873, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (36105504..36107567, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (35988360..35990423, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene keratin 18 pseudogene 14 Neighboring gene uncharacterized LOC124902661 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3265 Neighboring gene low density lipoprotein receptor class A domain containing 3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4628 Neighboring gene NANOG hESC enhancer GRCh37_chr11:35999121-35999622 Neighboring gene NANOG hESC enhancer GRCh37_chr11:36008240-36008741 Neighboring gene ribosomal protein L12 pseudogene 31 Neighboring gene microRNA 3973

    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)

    See Variation Viewer (GRCh38)

    General gene information

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    Other Names

    • WEE1 homolog 2 pseudogene
    • WEE2 oocyte meiosis inhibiting kinase

    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_024328.2 

      Range
      1..2064
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      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_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      35966810..35968873 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      36105504..36107567 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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