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    HNRNPA1P12 heterogeneous nuclear ribonucleoprotein A1 pseudogene 12 [ Homo sapiens (human) ]

    Gene ID: 644037, updated on 17-Sep-2024

    Summary

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    Official Symbol
    HNRNPA1P12provided by HGNC
    Official Full Name
    heterogeneous nuclear ribonucleoprotein A1 pseudogene 12provided by HGNC
    Primary source
    HGNC:HGNC:39130
    See related
    AllianceGenome:HGNC:39130
    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 HNRNPA1P12 in Genome Data Viewer
    Location:
    5q14.1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (80358880..80360099, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (80842854..80844073, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (79654699..79655918, complement)

    Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene RBMX2 pseudogene 5 Neighboring gene mediator complex subunit 27 pseudogene Neighboring gene RNA, U6 small nuclear 211, pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr5:79703845-79704643 Neighboring gene zinc finger FYVE-type containing 16 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16139 Neighboring gene FAM151B divergent transcript

    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)

    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_021856.2 

      Range
      101..1320
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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
      80358880..80360099 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060929.1 Alternate T2T-CHM13v2.0

      Range
      80842854..80844073 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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