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    BUB3P1 BUB3 mitotic checkpoint protein pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 646614, updated on 10-Oct-2023

    Summary

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    Official Symbol
    BUB3P1provided by HGNC
    Official Full Name
    BUB3 mitotic checkpoint protein pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:51559
    See related
    AllianceGenome:HGNC:51559
    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:
    7q31.1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (108993718..108995060, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (110318198..110319540, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (108633775..108635117, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986836 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:108465150-108466349 Neighboring gene long intergenic non-protein coding RNA 2903 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:108852947-108853448 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:108853449-108853948 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:108871548-108872106 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:109237086-109237867 Neighboring gene NANOG hESC enhancer GRCh37_chr7:109251582-109252157 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:109287079-109288278 Neighboring gene immunoglobulin binding protein 1 pseudogene Neighboring gene CTD small phosphatase 2 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_009438.3 

      Range
      101..1443
      Download
      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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      108993718..108995060 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      110318198..110319540 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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