Description

Werner syndrome homolog (human) [Source:MGI Symbol;Acc:MGI:109635]

Location
INSDC coordinates

chromosome:GRCm38:CM001001.2:33234384:33385527:1

Transcripts

This gene has 2 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDLengthProteinBiotypeCCDSUniProtRefSeqFlags
Wrn-201ENSMUST000000339906372 bp1401 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS22229O09053 Q3TB25 Q8BWH5
NM_011721
NP_035851
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Wrn-202ENSMUST000000339916262 bp1401 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS22229O09053 Q3TB25 Q8BWH5
NM_001122822
NP_001116294
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays