Welcome
{{ username}}
Message Center
{{ messageCount }} Messages
Go to Message Center
Watched Genes
{{$index + 1}}.
{{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Modify Subscription
Unsubscribe
Watched Ontology Terms
{{$index + 1}}.
{{ watchedTerm.term }} ({{watchedTerm.accId}})
Modify Subscription
Unsubscribe
{{gene.symbol}}:
{{ gene.description }}
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
{{ loginError }}
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be sent 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
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
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)
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
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
Scn4a
and
paramyotonia congenita of Von Eulenburg
in Ictidomys tridecemlineatus.
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
SCN4A (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
paramyotonia congenita of Von Eulenburg
(DOID:0111538)
0
papers in RGD have been used to annotate
Scn4a
An association has been curated linking
Scn4a
and
paramyotonia congenita of Von Eulenburg
in Ictidomys tridecemlineatus.
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
SCN4A (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
paramyotonia congenita of Von Eulenburg
(DOID:0111538)
0
papers in RGD have been used to annotate
Scn4a
Curation Notes: ClinVar Annotator: match by term: Paramyotonia congenita of Von Eulenburg | ClinVar Annotator: match by term: Von Eulenburg paramyotonia congenita
Original References(s):
PMID:10206477
PMID:10218481
PMID:10227633
PMID:10366610
PMID:10944223
PMID:11309455
PMID:11558801
PMID:11723275
PMID:11744749
PMID:11912116
PMID:11971097
PMID:12483017
PMID:12552059
PMID:12562902
PMID:12872329
PMID:12898257
PMID:12933953
PMID:1310898
PMID:1316765
PMID:1338909
PMID:14504341
PMID:14518676
PMID:14617673
PMID:14635102
PMID:15318338
PMID:15389891
PMID:15482957
PMID:15534250
PMID:15583983
PMID:15596759
PMID:15642860
PMID:15774523
PMID:15790667
PMID:16392038
PMID:1659948
PMID:16624558
PMID:16786525
PMID:16801039
PMID:16832098
PMID:16870577
PMID:17330043
PMID:17334961
PMID:17395131
PMID:17576681
PMID:17591984
PMID:17823953
PMID:17998485
PMID:18033047
PMID:18046642
PMID:18166706
PMID:18337100
PMID:18337730
PMID:18414213
PMID:18690054
PMID:18824591
PMID:19015492
PMID:19052238
PMID:19077043
PMID:19118277
PMID:1918277
PMID:19201608
PMID:19225109
PMID:19770477
PMID:19840739
PMID:20076800
PMID:20301669
PMID:20445432
PMID:20522878
PMID:20660662
PMID:20681998
PMID:20713951
PMID:20981092
PMID:21189962
PMID:21220685
PMID:21317558
PMID:21490317
PMID:21520339
PMID:2173143
PMID:21841462
PMID:22094069
PMID:22250216
PMID:22253644
PMID:22253645
PMID:22257501
PMID:22507243
PMID:22643347
PMID:22653516
PMID:22926674
PMID:23019082
PMID:23417379
PMID:23473731
PMID:23516313
PMID:23589580
PMID:23771340
PMID:23810313
PMID:23884711
PMID:23958773
PMID:24324661
PMID:24939454
PMID:25024265
PMID:25088311
PMID:25213595
PMID:25311598
PMID:25483584
PMID:25724373
PMID:25741868
PMID:25741909
PMID:25755818
PMID:25839108
PMID:26036855
PMID:26080010
PMID:26220970
PMID:26252573
PMID:26256659
PMID:26423924
PMID:26427606
PMID:26467025
PMID:26484179
PMID:2649440
PMID:26494408
PMID:26700687
PMID:26834636
PMID:26885337
PMID:26944947
PMID:27199537
PMID:27415035
PMID:27486940
PMID:27714768
PMID:27858759
PMID:28024841
PMID:28150151
PMID:28325641
PMID:28330959
PMID:28492532
PMID:28662944
PMID:28779239
PMID:29050397
PMID:29419865
PMID:29605429
PMID:29606556
PMID:29774303
PMID:29790872
PMID:29991727
PMID:30028520
PMID:30038349
PMID:30172468
PMID:30390395
PMID:30611854
PMID:30647473
PMID:30931713
PMID:31127727
PMID:31567646
PMID:31772215
PMID:32026975
PMID:32276507
PMID:32528171
PMID:32660787
PMID:32670189
PMID:32849172
PMID:33263785
PMID:33325393
PMID:33573884
PMID:34008892
PMID:34418069
PMID:35350395
PMID:35866763
PMID:36782059
PMID:7473241
PMID:7676326
PMID:7695243
PMID:7809121
PMID:7965854
PMID:7980103
PMID:8005599
PMID:8044656
PMID:8110459
PMID:8242056
PMID:8308722
PMID:8388676
PMID:8580427
PMID:8583225
PMID:8740371
PMID:8833340
PMID:8902732
PMID:8910215
PMID:9130156
PMID:9266738
PMID:9392583
PMID:9508833
PMID:9536098
PMID:9660885
PMID:9771789
PMID:9886942
Go Back to source page
Continue to Ontology report