Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | F13A1 | Bonobo | combined oxidative phosphorylation deficiency 14 | | ISO | F13A1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Combined oxidative phosphorylation deficiency 14 | ClinVar | PMID:22833457 and PMID:28492532 | F13A1 | Bonobo | factor XIII deficiency | | ISO | F13A1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary factor XIII deficiency disease | ClinVar | PMID:31136071 | F13A1 | Bonobo | Factor XIII, A Subunit, Deficiency Of | | ISO | F13A1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10027709 more ... | F13A1 | Bonobo | genetic disease | | ISO | F13A1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | F13A1 | Bonobo | hemorrhagic disease | | ISO | F13A1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Abnormal bleeding | ClinVar | | F13A1 | Bonobo | myocardial infarction | | ISO | F13A1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Myocardial infarction and protection against | ClinVar | PMID:10365735 more ... | F13A1 | Bonobo | thrombophilia due to thrombin defect | | ISO | F13A1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Thrombophilia due to thrombin defect | ClinVar | PMID:22995991 and PMID:9531026 | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
 |
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 - CTD
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