Human (GRCh38.p14)
Description

double homeobox 4 [Source:HGNC Symbol;Acc:HGNC:50800]

Location

Chromosome 4: 190,173,774-190,185,942 forward strand.

GRCh38:CM000666.2

View alleles of this gene on alternative sequences

About this gene

This gene has 6 transcripts (splice variants), 1 gene allele, 235 orthologues, 50 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000565211.1DUX4-2031710424aaENSP00000458065.1
 
Protein coding
CCDS77990Q9UBX2-1 NM_001306068.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000569241.5DUX4-2041574424aaENSP00000456539.1
 
Protein coding
CCDS77990Q9UBX2-1 -GENCODE basicAPPRIS P2TSL:1
ENST00000616166.1DUX4-2061275424aaENSP00000483555.1
 
Protein coding
CCDS77990Q9UBX2-1 -GENCODE basicAPPRIS P2TSL:NA
ENST00000570263.5DUX4-205768160aaENSP00000455112.1
 
Protein coding
CCDS93681Q9UBX2-2 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000564366.2DUX4-202387No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000563716.5DUX4-201285No protein-
 
Protein coding CDS not defined
--TSL:5