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FCMTE2 familial cortical myoclonic tremor with epilepsy 2 [ Homo sapiens (human) ]

Gene ID: 554188, discontinued on 15-Mar-2023
Gene symbol
FCMTE2
Gene description
familial cortical myoclonic tremor with epilepsy 2
See related
MIM:607876
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FAME; ADCME; FAME2; BAFME2
Location:
2p11.1-q12.2
familial cortical myoclonic tremor with epilepsy 2

Markers

Other Names

  • benign adult familial myoclonic epilepsy 2
  • cortical myoclonus and epilepsy, autosomal dominant
  • familial adult myoclonic epilepsy 2

Property

  • phenotype only