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 IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Wrn-201ENSMUST0000003399063721401 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS22229O09053 Q3TB25 Q8BWH5
NM_011721
NP_035851
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PIAPPRIS principal isoform [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Wrn-202ENSMUST0000003399162621401 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS22229O09053 Q3TB25 Q8BWH5
NM_001122822
NP_001116294
TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PIAPPRIS principal isoform [04-09-2014]
Glossary entry for APPRIS
APPRIS website

Gene-based displays