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DUX4L10 double homeobox 4 like 10 (pseudogene) [ Homo sapiens (human) ]

Gene ID: 440013, updated on 13-May-2022

Summary

Official Symbol
DUX4L10provided by HGNC
Official Full Name
double homeobox 4 like 10 (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:31354
See related
Ensembl:ENSG00000278664 AllianceGenome:HGNC:31354
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
DUX10
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Genomic context

See DUX4L10 in Genome Data Viewer
Location:
10q26.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (133743330..133744608)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (134707958..134709236)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (135480655..135481933)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene double homeobox 4 like 20 (pseudogene) Neighboring gene double homeobox 4 like 29 (pseudogene) Neighboring gene double homeobox 4 like 11 (pseudogene) Neighboring gene double homeobox 4 like 12 (pseudogene)

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_012775.4 

    Range
    101..1379
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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
    133743330..133744608
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    134707958..134709236
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)