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

Gene ID: 554188, discontinued on 15-Mar-2023

Summary

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Official Symbol
FCMTE2provided by HGNC
Official Full Name
familial cortical myoclonic tremor with epilepsy 2provided by HGNC
Primary source
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

Genomic context

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Location:
2p11.1-q12.2

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
familial cortical myoclonic tremor with epilepsy 2
OMIM: 607876GeneReviews: Not available

General gene information

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Markers

Other Names

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

Property

  • phenotype only

Gene LinkOut

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