Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Wrn MGP_SPRETEiJ_G0032079

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Description

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

Location

Chromosome 8: 30,778,819-30,950,134 reverse strand.

SPRET_EiJ_v1:CM004101.1

About this gene

This gene has 3 transcripts (splice variants), 152 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
MGP_SPRETEiJ_T0087611.1	Wrn-202	6352	1401aa	MGP_SPRETEiJ_P0087611	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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_SPRETEiJ_T0087612.1	Wrn-203	6242	1401aa	MGP_SPRETEiJ_P0087612	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
MGP_SPRETEiJ_T0087610.1	Wrn-201	1105	326aa	MGP_SPRETEiJ_P0087610	Unknown likely coding	-

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Summary

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