×
Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Update Watcher
Remove Watcher
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Update Watcher
Remove Watcher
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
×
Save what matters to you
{{ loginError }}
Sign in with your RGD account
Email Address:
Password:
Create New Account
Recover Password
×
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be send to {{ username }}
{{geneWatchAttr}}
Analyze
Gene
Strain
QTL
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)
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
Community Projects
(beta)
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
(beta)
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)
Diseases
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
Phenotypes & Models
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
GERRC (Gene Editing Rat Resource Center)
Phenotypes in Other Animal Models
Animal Husbandry
Strain Medical Records
Phylogenetics
Strain Availability
Calendar
Rats 101
Submissions
Photo Archive
Pathways
Community
Rat Community Forum
Directory of Rat Laboratories
Video Tutorials
News
RGD Publications
RGD Presentations Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
View As List
View As Table
GENE - TERM ANNOTATION REPORT
2 Annotations Found.
An association has been curated linking
Atp1a3
and
Alternating Hemiplegia of Childhood 2
in Rattus norvegicus.
The association was
inferred from sequence orthology
(ISO)
The annotation was made from
OMIM Disease Annotation Pipeline
The annotation has been inferred from sequence orthology with
ATP1A3 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
Alternating Hemiplegia of Childhood 2
(DOID:9001300)
30
papers in RGD have been used to annotate
Atp1a3
An association has been curated linking
Atp1a3
and
Alternating Hemiplegia of Childhood 2
in Rattus norvegicus.
The association was
inferred from sequence orthology
(ISO)
The annotation was made from
RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
The annotation has been inferred from sequence orthology with
ATP1A3 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
Alternating Hemiplegia of Childhood 2
(DOID:9001300)
30
papers in RGD have been used to annotate
Atp1a3
Curation Notes: ClinVar Annotator: match by term: Alternating hemiplegia of childhood 2
Original References(s):
PMID:11061257
PMID:12112218
PMID:15260953
PMID:15390049
PMID:16199547
PMID:16632466
PMID:17282997
PMID:17516473
PMID:17576681
PMID:17595045
PMID:18414213
PMID:19652145
PMID:20301294
PMID:20576601
PMID:21911500
PMID:22534615
PMID:22842232
PMID:22850527
PMID:22924536
PMID:23409136
PMID:23483595
PMID:24100174
PMID:24123283
PMID:24431296
PMID:24468074
PMID:24523486
PMID:24631656
PMID:24793181
PMID:24842602
PMID:24983657
PMID:24996492
PMID:25056583
PMID:25447930
PMID:25523819
PMID:25656163
PMID:25681536
PMID:25741868
PMID:25895915
PMID:25996915
PMID:26297560
PMID:26400718
PMID:26410222
PMID:26417536
PMID:26453127
PMID:26467025
PMID:26633545
PMID:26993267
PMID:27146299
PMID:27268479
PMID:27626066
PMID:27634470
PMID:27726050
PMID:28293679
PMID:28441826
PMID:28492532
PMID:28500446
PMID:28637637
PMID:28647130
PMID:28849312
PMID:28901192
PMID:29066118
PMID:29302074
PMID:29305691
PMID:29397530
PMID:29915382
PMID:30071271
PMID:30657467
PMID:31425744
PMID:31616254
PMID:31942761
PMID:32454213
PMID:32581362
PMID:34008892
PMID:34342181
PMID:35047275
PMID:8733056
PMID:9536098
Go Back to source page
Continue to Ontology report