Human (GRCh38.p14)
Description

DNA damage inducible 1 homolog 2 [Source:HGNC Symbol;Acc:HGNC:24578]

Gene Synonyms

MGC14844

Location

Chromosome 1: 15,617,458-15,669,044 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 8 transcripts (splice variants), 158 orthologues and 4 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000480945.6DDI2-20210667399aaENSP00000417748.1
 
Protein coding
CCDS30607Q5TDH0-1 NM_032341.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000711099.1DDI2-20810665418aaENSP00000518577.1
 
Protein coding
--GENCODE basic
ENST00000711098.1DDI2-207106041022aaENSP00000518576.1
 
Protein coding
--GENCODE basic
ENST00000320153.10DDI2-201207699aaENSP00000449475.1
 
Nonsense mediated decay
H0YII4 -TSL:2CDS 5' incomplete
ENST00000483899.1DDI2-203497103aaENSP00000448878.1
 
Nonsense mediated decay
H0YI90 -TSL:3CDS 5' incomplete
ENST00000486680.1DDI2-2041501No protein-
 
Retained intron
--TSL:1
ENST00000548451.1DDI2-206625No protein-
 
Retained intron
--TSL:5
ENST00000546927.1DDI2-205592No protein-
 
Retained intron
--TSL:2