Homo sapiens Gene: EPM2AIP1
Summary
InnateDB Gene IDBG-116451.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol EPM2AIP1
Gene Name EPM2A (laforin) interacting protein 1
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000178567
Encoded Proteins
EPM2A (laforin) interacting protein 1
EPM2A (laforin) interacting protein 1
EPM2A (laforin) interacting protein 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 3:36985043-36993168
Strand Reverse strand
Band p22.2
Transcripts
ENST00000322716 ENSP00000406027
ENST00000623924 ENSP00000485489
ENST00000624586 ENSP00000485091
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
Experimentally validated
Total 8 [view]
Protein-Protein 5 [view]
Protein-DNA 3 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0032868 response to insulin
GO:0045725 positive regulation of glycogen biosynthetic process
GO:2000467 positive regulation of glycogen (starch) synthase activity
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005783 endoplasmic reticulum
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q7L775
TrEMBL
UniProt Splice Variant
Entrez Gene 9852
UniGene Hs.28020 Hs.593145 Hs.601968 Hs.607921
RefSeq NM_014805
HUGO HGNC:19735
OMIM 607911
CCDS CCDS46790
HPRD
IMGT
EMBL AB018309 AF059751 AY178832 BC064696
GenPept AAG43120 AAH64696 AAO21376 BAA34486
RNA Seq Atlas 9852