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Aliases for FCMTE2 Gene

Aliases for FCMTE2 Gene

  • Familial Cortical Myoclonic Tremor With Epilepsy 2 2 3
  • Cortical Myoclonus And Epilepsy, Autosomal Dominant 2 3
  • Benign Adult Familial Myoclonic Epilepsy 2 2 3
  • Familial Adult Myoclonic Epilepsy 2 2 3
  • BAFME2 3
  • FAME2 3
  • ADCME 3
  • FAME 3

External Ids for FCMTE2 Gene

Summaries for FCMTE2 Gene

GeneCards Summary for FCMTE2 Gene

FCMTE2 (Familial Cortical Myoclonic Tremor With Epilepsy 2) is a Genetic Locus. Diseases associated with FCMTE2 include Benign Adult Familial Myoclonic Epilepsy.

Additional gene information for FCMTE2 Gene

No data available for Entrez Gene Summary , CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for FCMTE2 Gene

Genomics for FCMTE2 Gene

Genomic Locations for FCMTE2 Gene

Genomic Locations for FCMTE2 Gene
Unknown strand

Genomic View for FCMTE2 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for FCMTE2 Gene

Proteins for FCMTE2 Gene

Post-translational modifications for FCMTE2 Gene

No Post-translational modifications

No data available for DME Specific Peptides for FCMTE2 Gene

Domains & Families for FCMTE2 Gene

Graphical View of Domain Structure for InterPro Entry

No data available for Gene Families , Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for FCMTE2 Gene

Function for FCMTE2 Gene

Animal Model Products

Clone Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for FCMTE2 Gene

Localization for FCMTE2 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS , Subcellular locations from the Human Protein Atlas (HPA) and Gene Ontology (GO) - Cellular Components for FCMTE2 Gene

Pathways & Interactions for FCMTE2 Gene

SuperPathways for FCMTE2 Gene

No Data Available

Interacting Proteins for FCMTE2 Gene

Gene Ontology (GO) - Biological Process for FCMTE2 Gene


No data available for Pathways by source and SIGNOR curated interactions for FCMTE2 Gene

Drugs & Compounds for FCMTE2 Gene

No Compound Related Data Available

Transcripts for FCMTE2 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for FCMTE2 Gene

No ASD Table

Relevant External Links for FCMTE2 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for FCMTE2 Gene

Expression for FCMTE2 Gene

NURSA nuclear receptor signaling pathways regulating expression of FCMTE2 Gene:

No Expression Related Data Available

No data available for mRNA expression in normal human tissues , mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners , mRNA Expression by UniProt/SwissProt , Evidence on tissue expression from TISSUES and Phenotype-based relationships between genes and organs from Gene ORGANizer for FCMTE2 Gene

Orthologs for FCMTE2 Gene

No data available for Orthologs and Evolution for FCMTE2 Gene

Paralogs for FCMTE2 Gene

No data available for Paralogs for FCMTE2 Gene

Variants for FCMTE2 Gene

Additional Variant Information for FCMTE2 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) and Variation tolerance for FCMTE2 Gene

Disorders for FCMTE2 Gene

MalaCards: The human disease database

(1) MalaCards diseases for FCMTE2 Gene - From: GeneCards

Disorder Aliases PubMed IDs
benign adult familial myoclonic epilepsy
  • adcme
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with FCMTE2: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for FCMTE2 Gene

Publications for FCMTE2 Gene

  1. Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2. (PMID: 11701600) Guerrini R … Casari G (Brain : a journal of neurology 2001) 2 3 58

Products for FCMTE2 Gene

Sources for FCMTE2 Gene

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