Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | FMR1 | Green Monkey | autistic disorder | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:21681106 more ... | FMR1 | Green Monkey | autosomal hemophilia A | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: AUTOSOMAL HEMOPHILIA A | ClinVar | PMID:31690835 | FMR1 | Green Monkey | factor VIII deficiency | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Factor 8 deficiency and congenital | ClinVar | PMID:31690835 | FMR1 | Green Monkey | fragile X syndrome | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fragile X syndrome | ClinVar | PMID:11445641 more ... | FMR1 | Green Monkey | fragile X-associated tremor/ataxia syndrome | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | FMR1 | Green Monkey | genetic disease | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:10448821 more ... | FMR1 | Green Monkey | intellectual disability | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Intellectual disability | ClinVar | PMID:25167861 and PMID:25741868 | FMR1 | Green Monkey | primary ovarian insufficiency | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Fragile x premature ovarian failure | ClinVar | PMID:25741868 | FMR1 | Green Monkey | primary ovarian insufficiency 1 | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FMR1-Related Primary Ovarian Insufficiency | ClinVar | PMID:25741868 | FMR1 | Green Monkey | syndromic X-linked intellectual disability Lubs type | | ISO | FMR1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type | ClinVar | PMID:22679399 more ... | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
 |
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 - MGI
Imported Disease Annotations - OMIM
Gene Ontology Annotations Click to see Annotation Detail View
Biological Process
Cellular Component
Molecular Function
