Description

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

Synonyms

RECQ3, RECQL2

Location
INSDC coordinates

chromosome:GRCh38:CM000670.2:31033801:31173769:1

Transcripts

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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Stable ID

ENSG00000165392.6

Status

Current

Latest Version

ENSG00000165392.6

Release: 76 (current)

Assembly: GRCh38

Database: homo_sapiens_core_76_38

Associated archived IDs for this stable ID version

No associated IDs found

Gene-based displays