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

Configure this page

Share this page

Bookmark this page

.

Gene: epm2a ENSXETG00000017691

.

Description

epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) [Source:Xenbase;Acc:XB-GENE-965638]

Location

Primary_assembly 5: 45,936,974-45,985,053 reverse strand.

UCB_Xtro_10.0:CM004447.2

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 27 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSXETT00000118963.1	epm2a-202	5392	340aa	ENSXETP00000103395.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A803J6D5	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,
ENSXETT00000038390.5	epm2a-201	4101	317aa	ENSXETP00000038390.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A803KJR0	-

.

Summary

.

.