Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

RGD ID: 1552242
Species: Mus musculus
RGD Object: Gene
Symbol: Eif2b3
Name: eukaryotic translation initiation factor 2B, subunit 3
Acc ID: DOID:9002704
Term: Leukoencephalopathies
Definition: Any of various diseases affecting the white matter of the central nervous system.
Definition Source(s): MESH:D056784
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Eif2b3 ISOEIF2B3 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: CACH syndrome | ClinVar Annotator: match by term: CACH/VWM syndromePMID:11835386 PMID:16807905 PMID:18263758 PMID:18414213 PMID:19158808 PMID:19909266 PMID:20301435 PMID:21484434 PMID:22312164 PMID:23932106 PMID:24028880 PMID:25079571 PMID:25326635 PMID:25741868 PMID:25761052 PMID:26162493 PMID:26467025 PMID:28492532 PMID:31072091
Eif2b3 ISOEIF2B3 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: CACH/VWM syndromePMID:11835386 PMID:16807905 PMID:18263758 PMID:18414213 PMID:19909266 PMID:20301435 PMID:22312164 PMID:23932106 PMID:24028880 PMID:25079571 PMID:25326635 PMID:25741868 PMID:25761052 PMID:26162493 PMID:26467025 PMID:28492532 PMID:31072091 PMID:31418856 PMID:31692161 PMID:32180488 PMID:33432707 PMID:33517449
Go Back to source page   Continue to Ontology report