Description

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

Synonyms

RECQ3, RECQL2

Location

Chromosome 8: 31,033,801-31,173,769 forward strand.

GRCh38:CM000670.2

About this gene

This gene has 3 transcripts (splice variants), 58 orthologues, 4 paralogues, is a member of 1 Ensembl protein family and is associated with 3 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
WRN-001ENST0000029813952151432aaENSP00000298139
 
Protein coding
CCDS6082Q14191 NM_000553
NP_000544
TSL:1GENCODE basicAPPRIS P1
WRN-002ENST000005216203593No protein-
 
Retained intron
---TSL:1
WRN-003ENST00000520169629No protein-
 
Retained intron
---TSL:3
Stable ID

ENSG00000165392.9

Status

Current

Latest Version

ENSG00000165392.9

Release: 81 (current)

Assembly: GRCh38

Database: homo_sapiens_core_81_38

Associated archived IDs for this stable ID version

No associated IDs found

Gene-based displays