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    HNRNPA1P64 heterogeneous nuclear ribonucleoprotein A1 pseudogene 64 [ Homo sapiens (human) ]

    Gene ID: 100129325, updated on 17-Sep-2024

    Summary

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    Official Symbol
    HNRNPA1P64provided by HGNC
    Official Full Name
    heterogeneous nuclear ribonucleoprotein A1 pseudogene 64provided by HGNC
    Primary source
    HGNC:HGNC:48794
    See related
    Ensembl:ENSG00000213559 AllianceGenome:HGNC:48794
    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 HNRNPA1P64 in Genome Data Viewer
    Location:
    1p31.1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (80450948..80452075, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (80288527..80289654, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (80916633..80917760, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene PAI-1 mRNA binding protein pseudogene Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr1:80603369-80603984 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:80647066-80647592 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_9048 Neighboring gene high mobility group box 1 pseudogene 18 Neighboring gene NANOG hESC enhancer GRCh37_chr1:80851257-80851786 Neighboring gene COX6A1 pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 1781

    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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    Markers

    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_032722.2 

      Range
      101..1228
      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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      80450948..80452075 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      80288527..80289654 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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    Research Materials