Gene: ENSCGRG00001016491

Description

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

Location

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCGRT00001020333.1	-	4203	1400aa	ENSCGRP00001016089.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C2MAZ8	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,

Summary