Werner syndrome RecQ like helicase [Source:MGI Symbol;Acc:MGI:109635]
Chromosome 8: 33,724,412-33,875,555 reverse strand.
GRCm39:CM001001.3
This gene has 4 transcripts (splice variants), 152 orthologues, 4 paralogues and is associated with 31 phenotypes.
Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | Flags |
---|---|---|---|---|---|---|---|---|
ENSMUST00000033991.13 | Wrn-202 | 6262 | 1401aa | ENSMUSP00000033991.7 | Protein coding | CCDS22229 | O09053 | Ensembl Canonical, GENCODE basic, APPRIS P1, TSL:5, |
ENSMUST00000033990.7 | Wrn-201 | 5019 | 1401aa | ENSMUSP00000033990.6 | Protein coding | CCDS22229 | O09053 | GENCODE basic, APPRIS P1, TSL:1, |
ENSMUST00000211498.2 | Wrn-204 | 4856 | 1158aa | ENSMUSP00000147379.2 | Protein coding | A0A1B0GR54 | GENCODE basic, TSL:1, | |
ENSMUST00000209293.2 | Wrn-203 | 1921 | No protein | - | Retained intron | - | TSL:1, |