Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | KCNE1 | Dog | amyotrophic lateral sclerosis type 1 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 1 | ClinVar | PMID:17237124 more ... | KCNE1 | Dog | arrhythmogenic right ventricular cardiomyopathy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | autosomal dominant intellectual developmental disorder 7 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: DYRK1A-related intellectual disability syndrome | ClinVar | PMID:17237124 more ... | KCNE1 | Dog | Brugada syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | Cardiac Arrhythmias | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cardiac arrhythmia | ClinVar | | KCNE1 | Dog | cardiomyopathy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cardiomyopathies | ClinVar | PMID:10807545 more ... | KCNE1 | Dog | cardiomyopathy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cardiomyopathies | ClinVar | PMID:10807545 more ... | KCNE1 | Dog | cardiomyopathy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10807545 more ... | KCNE1 | Dog | cardiomyopathy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10807545 more ... | KCNE1 | Dog | dilated cardiomyopathy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Primary dilated cardiomyopathy | ClinVar | PMID:25741868 more ... | KCNE1 | Dog | Familial Platelet Disorder with Associated Myeloid Malignancy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:17237124 more ... | KCNE1 | Dog | Hearing Loss | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hearing loss and deafness | ClinVar | | KCNE1 | Dog | Hearing Loss, Noise-Induced | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Noise induced hearing loss | ClinVar | PMID:12402336 more ... | KCNE1 | Dog | hypertrophic cardiomyopathy | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy | ClinVar | PMID:24217263 and PMID:28492532 | KCNE1 | Dog | immunodeficiency 28 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Immunodeficiency 28 | ClinVar | PMID:17237124 more ... | KCNE1 | Dog | Jervell And Lange-Nielsen Syndrome 2 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jervell and Lange-Nielsen syndrome 2 | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | Jervell-Lange Nielsen syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Jervell and Lange-Nielsen syndrome | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome 1 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ventricular fibrillation with prolonged QT interval | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome 1 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ventricular fibrillation with prolonged QT interval | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome 1 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ventricular fibrillation with prolonged QT interval | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome 1 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ventricular fibrillation with prolonged QT interval | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome 1 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ventricular fibrillation with prolonged QT interval | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome 1 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | Long QT Syndrome 2/5 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Long QT syndrome 2/5 and digenic | ClinVar | PMID:10807545 more ... | KCNE1 | Dog | long QT syndrome 5 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | long QT syndrome 6 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Long QT syndrome 6 | ClinVar | PMID:21626672 more ... | KCNE1 | Dog | Parkinson's disease 20 | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Early-onset Parkinson disease 20 | ClinVar | PMID:28492532 | KCNE1 | Dog | Romano-Ward Syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | Sudden Death | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden unexplained death | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | sudden infant death syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SUDDEN INFANT DEATH SYNDROME | ClinVar | PMID:25741868 more ... | KCNE1 | Dog | Sudden Unexpected Nocturnal Death Syndrome | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden unexpected nocturnal death syndrome | ClinVar | PMID:10400998 more ... | KCNE1 | Dog | thrombocytopenia | | ISO | KCNE1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Thrombocytopenia | ClinVar | PMID:32581362 | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
 |
Welcome {{ username}}
Message Center
{{ messageCount }} Messages
Watched Genes
{{$index + 1}}. {{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Watched Ontology Terms
{{gene.symbol}}: {{ gene.description }}
|
| You must be logged in to use this feature |
| {{ loginError }} |
|
|
Analyze GeneStrainQTL List |
 Gene Annotator (Functional Annotation) unavailable |
 Gene Annotator (Annotation Distribution) unavailable |
 Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable |
Gene Annotator (Functional Annotation) |
Gene Annotator (Annotation Distribution) |
Variant Visualizer (Genomic Variants) |
 InterViewer (Protein-Protein Interactions) unavailable |
 Gviewer (Genome Viewer) unavailable |
 Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable |
InterViewer (Protein-Protein Interactions) |
GViewer (Genome Viewer) |
Variant Visualizer (Damaging Variants) |
 Gene Annotator (Annotation Comparison) unavailable |
 OLGA (Gene List Generator) unavailable |
 |
Gene Annotator (Annotation Comparison) |
OLGA (Gene List Generator) |
Excel (Download) |
 MOET (Multi-Ontology Enrichement) unavailable |
 GOLF (Gene-Ortholog Location Finder) unavailable |
|
MOET (Multi-Ontology Enrichement) |
GOLF (Gene-Ortholog Location Finder) |
Imported Disease Annotations - OMIM
Gene Ontology Annotations Click to see Annotation Detail View
Biological Process
Cellular Component
Molecular Function
Molecular Pathway Annotations Click to see Annotation Detail View
