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
TSC2
and
tuberous sclerosis
in Sus scrofa.
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
TSC2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
173
RGD objects have been annotated to
tuberous sclerosis
(DOID:13515)
0
papers in RGD have been used to annotate
TSC2
Curation Notes: ClinVar Annotator: match by term: Cortical tubers | ClinVar Annotator: match by term: Tuberous sclerosis syndrome
Original References(s):
PMID:10069705
PMID:10090883
PMID:10205261
PMID:10206124
PMID:10215407
PMID:10227394
PMID:10330349
PMID:10533066
PMID:10533067
PMID:10570911
PMID:10577937
PMID:10607950
PMID:10633137
PMID:10732801
PMID:10735580
PMID:10823953
PMID:10905251
PMID:10942116
PMID:11068191
PMID:11112665
PMID:1112665
PMID:11208653
PMID:11290735
PMID:11403047
PMID:11437991
PMID:11468687
PMID:11520734
PMID:11521203
PMID:11603814
PMID:11741832
PMID:11741833
PMID:11810271
PMID:11829138
PMID:12015165
PMID:12062115
PMID:12086608
PMID:12111193
PMID:12136241
PMID:12235314
PMID:12511557
PMID:12752578
PMID:12906785
PMID:12913212
PMID:14508401
PMID:14641237
PMID:14718525
PMID:14756965
PMID:14993219
PMID:15024740
PMID:15072102
PMID:15121792
PMID:15121797
PMID:1520333
PMID:15236319
PMID:15483652
PMID:15595939
PMID:15712319
PMID:15798777
PMID:15874888
PMID:15963462
PMID:16032769
PMID:16042315
PMID:16114042
PMID:16129702
PMID:16199547
PMID:16237225
PMID:16417848
PMID:16464865
PMID:16554133
PMID:16822245
PMID:16877242
PMID:16981987
PMID:17034546
PMID:17120248
PMID:17304050
PMID:17536269
PMID:17576681
PMID:17681840
PMID:18032745
PMID:18302728
PMID:18308511
PMID:18410267
PMID:18411301
PMID:18414213
PMID:18550814
PMID:18695678
PMID:1870099
PMID:18772611
PMID:18792920
PMID:18830229
PMID:18854862
PMID:19254590
PMID:19258292
PMID:19259131
PMID:19369101
PMID:19419980
PMID:19747374
PMID:19823873
PMID:20108343
PMID:20165957
PMID:20301399
PMID:2039137
PMID:20399389
PMID:20498439
PMID:20633017
PMID:21309039
PMID:21332470
PMID:21407264
PMID:21418539
PMID:21510812
PMID:21520333
PMID:21567926
PMID:21624971
PMID:21811971
PMID:21846442
PMID:21910228
PMID:22055460
PMID:22161988
PMID:22189265
PMID:22343534
PMID:22490766
PMID:22552000
PMID:22558107
PMID:22703879
PMID:22707510
PMID:22805177
PMID:22867869
PMID:22903760
PMID:22974335
PMID:22995991
PMID:23006675
PMID:23217510
PMID:23254740
PMID:23389244
PMID:23504366
PMID:23514105
PMID:23955302
PMID:24033266
PMID:24055113
PMID:24271014
PMID:24412076
PMID:24668795
PMID:24728327
PMID:24789117
PMID:25039834
PMID:25058500
PMID:25088526
PMID:25180276
PMID:25203624
PMID:25231023
PMID:25281918
PMID:25338684
PMID:25401301
PMID:25432535
PMID:25498131
PMID:25525159
PMID:25593300
PMID:25599672
PMID:25637381
PMID:25724664
PMID:25741868
PMID:25741905
PMID:25782670
PMID:25862857
PMID:25892863
PMID:25911330
PMID:25927202
PMID:26155992
PMID:26332594
PMID:26467025
PMID:26489027
PMID:26540169
PMID:26563443
PMID:26580448
PMID:26633542
PMID:26637798
PMID:26703369
PMID:26994145
PMID:27060308
PMID:27078846
PMID:27153395
PMID:27174333
PMID:27176796
PMID:27194594
PMID:27406250
PMID:27493206
PMID:27494029
PMID:27600092
PMID:27601542
PMID:27621404
PMID:27757534
PMID:27774772
PMID:27859028
PMID:27884173
PMID:27930734
PMID:28065512
PMID:28074849
PMID:28087349
PMID:28127866
PMID:28149746
PMID:28178598
PMID:28202063
PMID:28211972
PMID:28250423
PMID:28397210
PMID:28409891
PMID:28492532
PMID:28505269
PMID:28600779
PMID:28623545
PMID:28643795
PMID:28771801
PMID:28786016
PMID:28968464
PMID:28991257
PMID:2903760
PMID:29101226
PMID:29167182
PMID:29196670
PMID:29221145
PMID:29271092
PMID:29286531
PMID:29308833
PMID:29344138
PMID:29432982
PMID:29458892
PMID:29476190
PMID:29500070
PMID:29641532
PMID:29642139
PMID:29655203
PMID:29659200
PMID:29740858
PMID:29801666
PMID:29925043
PMID:29932062
PMID:29933521
PMID:30024541
PMID:30036593
PMID:30093976
PMID:30185235
PMID:30255984
PMID:30548481
PMID:30564305
PMID:30583724
PMID:30712878
PMID:30787465
PMID:30986793
PMID:31005478
PMID:31018109
PMID:31291687
PMID:31370276
PMID:31375768
PMID:31444548
PMID:31586081
PMID:31591157
PMID:31655562
PMID:31785789
PMID:31799751
PMID:31819260
PMID:31855466
PMID:31856217
PMID:31927531
PMID:32005694
PMID:32211034
PMID:32216820
PMID:32313033
PMID:32382396
PMID:32410215
PMID:32461669
PMID:32461694
PMID:32502382
PMID:32555378
PMID:32581362
PMID:32830346
PMID:32860008
PMID:32917028
PMID:32917966
PMID:33051600
PMID:33074564
PMID:33391346
PMID:33532864
PMID:34070849
PMID:34145886
PMID:34246755
PMID:34252879
An association has been curated linking
TSC2
and
tuberous sclerosis
in Sus scrofa.
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
TSC2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
173
RGD objects have been annotated to
tuberous sclerosis
(DOID:13515)
0
papers in RGD have been used to annotate
TSC2
Curation Notes: ClinVar Annotator: match by term: Cortical tubers | ClinVar Annotator: match by term: Tuberous sclerosis syndrome
Original References(s):
PMID:34403804
PMID:34489640
PMID:34575676
PMID:34754157
PMID:34804623
PMID:34849272
PMID:35441217
PMID:35712104
PMID:35768438
PMID:35918040
PMID:36232477
PMID:37228977
PMID:4461062
PMID:5279523
PMID:7581393
PMID:7823706
PMID:8634701
PMID:8824881
PMID:8825048
PMID:9076719
PMID:9242607
PMID:9285776
PMID:9302281
PMID:9328481
PMID:9361032
PMID:9412784
PMID:9452050
PMID:9463313
PMID:9536098
PMID:9829910
PMID:9881533
Go Back to source page
Continue to Ontology report