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
DSG2
and
dilated cardiomyopathy 1BB
in Canis lupus familiaris.
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
DSG2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
4
RGD objects have been annotated to
dilated cardiomyopathy 1BB
(DOID:0110458)
1
papers in RGD have been used to annotate
DSG2
An association has been curated linking
DSG2
and
dilated cardiomyopathy 1BB
in Canis lupus familiaris.
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
DSG2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
4
RGD objects have been annotated to
dilated cardiomyopathy 1BB
(DOID:0110458)
1
papers in RGD have been used to annotate
DSG2
Curation Notes: ClinVar Annotator: match by term: DSG2-related condition | ClinVar Annotator: match by term: Dilated cardiomyopathy 1BB | ClinVar Annotator: match by term: Familial isolated dilated cardiomyopathy
Original References(s):
PMID:12586364
PMID:16025435
PMID:16199547
PMID:16773573
PMID:17105751
PMID:17576681
PMID:18382419
PMID:18678517
PMID:19039334
PMID:19358943
PMID:19569224
PMID:19863551
PMID:19955750
PMID:20031616
PMID:20031617
PMID:20152563
PMID:20197793
PMID:2040044
PMID:20400443
PMID:20603720
PMID:20708101
PMID:20716751
PMID:20857253
PMID:20864495
PMID:21397041
PMID:21455723
PMID:21606390
PMID:21606396
PMID:21636032
PMID:21859740
PMID:22214898
PMID:22458570
PMID:23071725
PMID:23137101
PMID:23299917
PMID:23381804
PMID:23396983
PMID:23671136
PMID:23810883
PMID:23810894
PMID:23812740
PMID:23861362
PMID:23871674
PMID:23871885
PMID:23889974
PMID:24033266
PMID:24055113
PMID:24070718
PMID:24082139
PMID:24125834
PMID:24503780
PMID:24704780
PMID:24967631
PMID:25087486
PMID:25172079
PMID:25209314
PMID:25213555
PMID:25332820
PMID:25351510
PMID:25445213
PMID:25525159
PMID:25637381
PMID:25741868
PMID:25820315
PMID:26138720
PMID:26220970
PMID:26230511
PMID:26498160
PMID:26656175
PMID:26688388
PMID:26743238
PMID:26822237
PMID:26850880
PMID:27055156
PMID:27194543
PMID:27532257
PMID:27930701
PMID:28074886
PMID:28087566
PMID:28254188
PMID:28254189
PMID:28255936
PMID:28341588
PMID:28471438
PMID:28492532
PMID:28588093
PMID:28600387
PMID:28818065
PMID:29038103
PMID:29178656
PMID:29343803
PMID:29456632
PMID:29544605
PMID:29566126
PMID:29750433
PMID:29790872
PMID:29802319
PMID:29899727
PMID:30177324
PMID:30391969
PMID:30790397
PMID:30830208
PMID:30847666
PMID:30885746
PMID:31019283
PMID:31042466
PMID:31386562
PMID:31402444
PMID:31447099
PMID:31542937
PMID:31737537
PMID:31845994
PMID:31983221
PMID:32102357
PMID:32268277
PMID:32569162
PMID:32659924
PMID:32665702
PMID:32682410
PMID:32746448
PMID:33029862
PMID:33232181
PMID:33460606
PMID:33500567
PMID:33552729
PMID:33652588
PMID:33673806
PMID:33821670
PMID:33919104
PMID:33949662
PMID:34317382
PMID:34500006
PMID:35087879
PMID:35300203
PMID:35819174
PMID:37418234
PMID:9536098
Go Back to source page
Continue to Ontology report