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    BTG4P1 BTG anti-proliferation factor 4 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 106480330, updated on 10-Dec-2024

    Summary

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    Official Symbol
    BTG4P1provided by HGNC
    Official Full Name
    BTG anti-proliferation factor 4 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:51544
    See related
    AllianceGenome:HGNC:51544
    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 BTG4P1 in Genome Data Viewer
    Location:
    5p14.1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (24786642..24787028, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (24891801..24892187, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (24786751..24787137, complement)

    Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene cadherin 10 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:24644784-24645379 Neighboring gene uncharacterized LOC124901174 Neighboring gene TRPC6 pseudogene 6 Neighboring gene long intergenic non-protein coding RNA 2239 Neighboring gene ReSE screen-validated silencer GRCh37_chr5:24985574-24985753 Neighboring gene Sharpr-MPRA regulatory region 953 Neighboring gene 5p14.1 distal LINE-mediated recombination region Neighboring gene long intergenic non-protein coding RNA 2228

    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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    Other Names

    • B-cell translocation gene 4 pseudogene 1

    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_044501.2 

      Range
      101..487
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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
      24786642..24787028 complement
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      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060929.1 Alternate T2T-CHM13v2.0

      Range
      24891801..24892187 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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