Gene: WRN ENSG00000165392

Description

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

Gene Synonyms

RECQ3, RECQL2, RECQL3

Location

GRCh37:CM000670.1

About this gene

This gene has 3 transcripts (splice variants), 4 paralogues and is associated with 68 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000298139.5	WRN-001	5215	1432aa	ENSP00000298139.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS6082	Q14191	NM_000553.4	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000521620.1	WRN-002	3593	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000520169.1	WRN-003	629	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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