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    HNRNPUP1 heterogeneous nuclear ribonucleoprotein U pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 319134, updated on 17-Sep-2024

    Summary

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    Official Symbol
    HNRNPUP1provided by HGNC
    Official Full Name
    heterogeneous nuclear ribonucleoprotein U pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:19931
    See related
    AllianceGenome:HGNC:19931
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HNRPUP
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    Genomic context

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    See HNRNPUP1 in Genome Data Viewer
    Location:
    14q21.2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (43300268..43300909)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (37491191..37491832)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (43769471..43770112)

    Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124903306 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:43531733-43532241 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_33884 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_33920 Neighboring gene tubulin beta pseudogene 3 Neighboring gene uncharacterized LOC105370470 Neighboring gene uncharacterized LOC124903307

    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_002512.4 

      Range
      101..742
      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_000014.9 Reference GRCh38.p14 Primary Assembly

      Range
      43300268..43300909
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060938.1 Alternate T2T-CHM13v2.0

      Range
      37491191..37491832
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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