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    DDX39AP1 DEAD-box helicase 39A pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 646164, updated on 10-Dec-2024

    Summary

    Official Symbol
    DDX39AP1provided by HGNC
    Official Full Name
    DEAD-box helicase 39A pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:39664
    See related
    AllianceGenome:HGNC:39664
    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

    See DDX39AP1 in Genome Data Viewer
    Location:
    13q12.12
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (22705237..22706212, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (21903307..21904282, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (23279376..23280351, complement)

    Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124903133 Neighboring gene Sharpr-MPRA regulatory region 3351 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr13:23126652-23127851 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:23218322-23218822 Neighboring gene ferritin heavy chain 1 pseudogene 7 Neighboring gene uncharacterized LOC124903254 Neighboring gene ribosomal protein L7a pseudogene 73

    Genomic regions, transcripts, and products

    General gene information

    Other Names

    • DEAD (Asp-Glu-Ala-Asp) box polypeptide 39 pseudogene
    • DEAD (Asp-Glu-Ala-Asp) box polypeptide 39A 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_011331.2 

      Range
      101..1076
      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_000013.11 Reference GRCh38.p14 Primary Assembly

      Range
      22705237..22706212 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060937.1 Alternate T2T-CHM13v2.0

      Range
      21903307..21904282 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)