Mouse (GRCm39)
Description

Werner syndrome RecQ like helicase [Source:MGI Symbol;Acc:MGI:109635]

Location
About this transcript

This transcript has 9 exons, is associated with 3696 variant alleles and maps to 77 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchFlags
ENSMUST00000033991.13Wrn-20262621401aaENSMUSP00000033991.7
 
Protein coding
CCDS22229O09053 Ensembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENSMUST00000033990.7Wrn-20150191401aaENSMUSP00000033990.6
 
Protein coding
CCDS22229O09053 GENCODE basicAPPRIS P1TSL:1
ENSMUST00000211498.2Wrn-20448561158aaENSMUSP00000147379.2
 
Protein coding
A0A1B0GR54 GENCODE basicTSL:1
ENSMUST00000209293.2Wrn-2031921No protein-
 
Retained intron
-TSL:1
Statistics

Exons: 9, Coding exons: 0, Transcript length: 1,921 bps,

Transcript Support Level (TSL)

TSL:1

Version

ENSMUST00000209293.2

Type

Retained intron

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.