Human (GRCh38.p14)
Description

defective in cullin neddylation 1 domain containing 3 [Source:HGNC Symbol;Acc:HGNC:28734]

Gene Synonyms

DKFZP686O0290, FLJ41725, MGC48972, SCCRO3

Location
About this transcript

This transcript has 3 exons, is annotated with 14 domains and features, is associated with 4082 variant alleles and maps to 215 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000324344.9DCUN1D3-2016136304aaENSP00000319482.3
 
Protein coding
CCDS10592Q8IWE4 NM_173475.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000563934.1DCUN1D3-2021996304aaENSP00000454762.1
 
Protein coding
CCDS10592Q8IWE4 -GENCODE basicAPPRIS P1TSL:5
Statistics

Exons: 3, Coding exons: 2, Transcript length: 1,996 bps, Translation length: 304 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8IWE4

CCDS

This transcript is a member of the Human CCDS set: CCDS10592

Transcript Support Level (TSL)

TSL:5

Version

ENST00000563934.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.