Human (GRCh38.p14)
Description

defective in cullin neddylation 1 domain containing 1 [Source:HGNC Symbol;Acc:HGNC:18184]

Gene Synonyms

DCUN1L1, RP42, SCCRO, SCRO, TES3

Location

Chromosome 3: 182,938,074-182,985,953 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 8 transcripts (splice variants), 223 orthologues and 4 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000292782.9DCUN1D1-2017849259aaENSP00000292782.4
 
Protein coding
CCDS3240Q96GG9 NM_020640.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000632685.1DCUN1D1-2083147244aaENSP00000488427.1
 
Protein coding
CCDS77862C9JVE2 -GENCODE basicTSL:1
ENST00000460412.6DCUN1D1-2022326244aaENSP00000419440.2
 
Protein coding
CCDS77862C9JVE2 -GENCODE basicTSL:3
ENST00000469954.5DCUN1D1-204970244aaENSP00000419359.1
 
Protein coding
CCDS77862C9JVE2 -GENCODE basicTSL:3
ENST00000487822.5DCUN1D1-20556092aaENSP00000418913.1
 
Protein coding
C9J0B2 -TSL:3CDS 3' incomplete
ENST00000497606.5DCUN1D1-207504128aaENSP00000417675.1
 
Protein coding
C9J8R4 -TSL:2CDS 3' incomplete
ENST00000466812.1DCUN1D1-20346175aaENSP00000420073.1
 
Protein coding
C9JRU6 -TSL:2CDS 3' incomplete
ENST00000492563.1DCUN1D1-20665935aaENSP00000418935.1
 
Nonsense mediated decay
F8WC32 -TSL:5