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DDX18P6 DEAD-box helicase 18 pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 100131370, updated on 10-Oct-2023

Summary

Official Symbol
DDX18P6provided by HGNC
Official Full Name
DEAD-box helicase 18 pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:31126
See related
AllianceGenome:HGNC:31126
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 DDX18P6 in Genome Data Viewer
Location:
10q23.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (91053009..91057025)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (91936682..91940699)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (92812766..92816782)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902479 Neighboring gene uncharacterized LOC105378430 Neighboring gene long intergenic non-protein coding RNA 502 Neighboring gene uncharacterized LOC105378429 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3760 Neighboring gene uncharacterized LOC124902481

Genomic regions, transcripts, and products

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_008704.2 

    Range
    101..4117
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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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    91053009..91057025
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    91936682..91940699
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    GenBank, FASTA, Sequence Viewer (Graphics)