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DDX10P2 DEAD-box helicase 10 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 401533, updated on 17-Sep-2024

Summary

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Official Symbol
DDX10P2provided by HGNC
Official Full Name
DEAD-box helicase 10 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:44961
See related
Ensembl:ENSG00000230360 AllianceGenome:HGNC:44961
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 DDX10P2 in Genome Data Viewer
Location:
9q21.32
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (82085641..82088850, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (94235270..94238479, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (84700556..84703765, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376107 Neighboring gene SPATA31 subfamily D member 1 Neighboring gene SPATA31 subfamily B member 1, pseudogene Neighboring gene ribosomal protein S2 pseudogene 34 Neighboring gene NANOG hESC enhancer GRCh37_chr9:84785175-84785704 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr9:84887382-84888581 Neighboring gene VISTA enhancer hs752 Neighboring gene VISTA enhancer hs800 Neighboring gene uncharacterized LOC112268046

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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Other Names

  • DEAD (Asp-Glu-Ala-Asp) box polypeptide 10 pseudogene 2

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_021626.5 

    Range
    101..3310
    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    82085641..82088850 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    94235270..94238479 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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