Summary
Sequence
Protein Information
- Protein summary
- Domains & features
- Variants
- PDB 3D protein model
- AlphaFold predicted model
Genetic Variation
- Variant table
- Variant image
- Population comparison
- Comparison image
External References
- General identifiers
- Oligo probes
Supporting evidence
ID History
- Transcript history
- Protein history

Custom tracks

Transcript: MGP_FVBNJ_T0088136.1

Description

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

Gene Synonyms

AI846146

Location

Reference strain equivalent

About this transcript

This transcript has 34 exons, is annotated with 44 domains and features and maps to 436 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
MGP_FVBNJ_T0088136.1	-	6338	1401aa	MGP_FVBNJ_P0088136	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS22229	O09053	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,
MGP_FVBNJ_T0088137.1	-	6228	1401aa	MGP_FVBNJ_P0088137	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	-

Protein summary