Free for academic non-profit institutions. Other users need a Commercial license

Aliases for EIM Gene

Aliases for EIM Gene

  • Infantile Myoclonic Epilepsy 3

External Ids for EIM Gene

Previous GeneCards Identifiers for EIM Gene

  • GC16U990136

Summaries for EIM Gene

GeneCards Summary for EIM Gene

EIM (Infantile Myoclonic Epilepsy) is a Genetic Locus. Diseases associated with EIM include Myoclonic Epilepsy Of Infancy.

Additional gene information for EIM 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 EIM Gene

Genomics for EIM Gene

Genomic Locations for EIM Gene

No location information available

Genomic View for EIM Gene


No data available for GeneHancer (GH) Regulatory Elements , Cytogenetic band and RefSeq DNA sequence for EIM Gene

Function for EIM Gene

Animal Model 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 EIM Gene

Localization for EIM 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 EIM Gene

Pathways & Interactions for EIM Gene

No Data Available

Interacting Proteins for EIM Gene

Gene Ontology (GO) - Biological Process for EIM Gene

None

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

Drugs & Compounds for EIM Gene

No Compound Related Data Available

Transcripts for EIM Gene

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

No ASD Table

No data available for mRNA/cDNA for EIM Gene

Expression for EIM 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 EIM Gene

Orthologs for EIM Gene

No data available for Orthologs and Evolution for EIM Gene

Paralogs for EIM Gene

No data available for Paralogs for EIM Gene

Variants for EIM Gene

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

Disorders for EIM Gene

MalaCards: The human disease database

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

Disorder Aliases PubMed IDs
myoclonic epilepsy of infancy
  • benign myoclonic epilepsy of infancy
- elite association - COSMIC cancer census association via MalaCards
Search EIM in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with EIM: view

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

Publications for EIM Gene

  1. Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13. (PMID: 10741954) Zara F … Bricarelli FD (American journal of human genetics 2000) 3 58

Products for EIM Gene

Sources for EIM Gene

Content
Loading form....