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DUX4L27 double homeobox 4 like 27 (pseudogene) [ Homo sapiens (human) ]

Gene ID: 100131369, updated on 29-Mar-2023

Summary

Official Symbol
DUX4L27provided by HGNC
Official Full Name
double homeobox 4 like 27 (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:50808
See related
Ensembl:ENSG00000258794 AllianceGenome:HGNC:50808
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 DUX4L27 in Genome Data Viewer
Location:
12p11.1
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (34208423..34209801, complement)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (34086057..34087435, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (34361358..34362736, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124903068 Neighboring gene RNA, 5S ribosomal pseudogene 357 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:34371322-34371822 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:34371823-34372323

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_021684.1 

    Range
    101..1479
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    34208423..34209801 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    34086057..34087435 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)