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DDX6P2 DEAD-box helicase 6 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100130117, updated on 10-Oct-2023

Summary

Official Symbol
DDX6P2provided by HGNC
Official Full Name
DEAD-box helicase 6 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:37806
See related
AllianceGenome:HGNC:37806
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

Location:
13q31.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (86275295..86277520)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (85477804..85480029)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (86927557..86929782)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene SLIT and NTRK like family member 6 Neighboring gene ReSE screen-validated silencer GRCh37_chr13:86428461-86428657 Neighboring gene Sharpr-MPRA regulatory region 1723 Neighboring gene MOB kinase activator 1A pseudogene 1 Neighboring gene NANOG hESC enhancer GRCh37_chr13:86736088-86736589 Neighboring gene uncharacterized LOC124903227 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr13:87010205-87011035 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:87015457-87015956 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr13:87015957-87016956 Neighboring gene NANOG hESC enhancer GRCh37_chr13:87017515-87018053 Neighboring gene uncharacterized LOC105370299

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • DEAD (Asp-Glu-Ala-Asp) box helicase 6 pseudogene 2
  • DEAD (Asp-Glu-Ala-Asp) box polypeptide 6 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_022972.3 

    Range
    1..2226
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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
    86275295..86277520
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    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_009646205.1 Reference GRCh38.p14 PATCHES

    Range
    17880..20105
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    85477804..85480029
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    GenBank, FASTA, Sequence Viewer (Graphics)