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EJM2 epilepsy, juvenile myoclonic 2 [ Homo sapiens (human) ]

Gene ID: 50715, updated on 2-Oct-2019

Summary

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Gene symbol
EJM2
Gene description
epilepsy, juvenile myoclonic 2
Primary source
MIM:604827
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
JME; EIG7

Genomic context

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Location:
15q14

Bibliography

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Related articles in PubMed

  1. Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. Elmslie FV, et al. Hum Mol Genet, 1997 Aug. PMID 9259280

GeneRIFs: Gene References Into Functions

Phenotypes

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epilepsy, juvenile myoclonic 2

General gene information

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Markers

Other Names

  • myoclonic epilepsy, juvenile, 2

Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases