Description

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

Synonyms

RECQ3, RECQL2

Location
Gene

This transcript is a product of gene ENSG00000165392

This gene has 3 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDLengthProteinBiotypeCCDSUniProtRefSeqFlags
WRN-001ENST000002981395215 bp1432 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS6082Q14191 NM_000553
NP_000544
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
WRN-002ENST000005216203593 bp No protein product
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
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WRN-003ENST00000520169629 bp No protein product
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
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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

Ensembl version

ENST00000298139.5

Type

Known protein coding

Prediction Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
GENCODE basic gene

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

Transcript-based displays