Description

Werner syndrome RecQ like helicase [Source:HGNC Symbol;Acc:HGNC:12791]

Synonyms

RECQ3, RECQL2

Location
About this transcript

This transcript has 35 exons, is annotated with 45 domains and features, is associated with 1289 variations and maps to 887 oligo probes.

Gene
NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
WRN-201ENST00000298139.552151432aaENSP00000298139
 
Protein coding
CCDS6082Q14191 NM_000553
NP_000544
TSL:1GENCODE basicAPPRIS P1
WRN-203ENST00000521620.53593No protein-
 
Retained intron
---TSL:1
WRN-202ENST00000520169.1629No protein-
 
Retained intron
---TSL:3
Statistics

Exons: 35, Coding exons: 34, Transcript length: 5,215 bps, Translation length: 1,432 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS6082

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q14191

Transcript Support Level (TSL)

TSL:1

Version

ENST00000298139.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Vega manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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

Transcript-based displays