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    ANKRD33BP2 ANKRD33B pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 100129384, updated on 10-Oct-2023

    Summary

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    Official Symbol
    ANKRD33BP2provided by HGNC
    Official Full Name
    ANKRD33B pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:56294
    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 ANKRD33BP2 in Genome Data Viewer
    Location:
    11p11.12
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (48900218..48901263, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (49068113..49069158, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (48921770..48922815, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene olfactory receptor family 4 subfamily A member 42 pseudogene Neighboring gene olfactory receptor family 4 subfamily A member 44 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr11:48827442-48828219 Neighboring gene NANOG hESC enhancer GRCh37_chr11:48837141-48837722 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:48838603-48839148 Neighboring gene OCT4 hESC enhancer GRCh37_chr11:48842688-48843189 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:48849408-48849948 Neighboring gene NANOG hESC enhancer GRCh37_chr11:48858585-48859086 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:48866441-48867079 Neighboring gene OCT4 hESC enhancer GRCh37_chr11:48895908-48896723 Neighboring gene tripartite motif containing 48 pseudogene Neighboring gene tripartite motif-containing 51C, pseudogene

    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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    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_028803.2 

      Range
      94..1139
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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
      48900218..48901263 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      49068113..49069158 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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