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
NF2
and
vestibular schwannomatosis
in Chlorocebus sabaeus.
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
NF2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
25
RGD objects have been annotated to
vestibular schwannomatosis
(DOID:0111252)
0
papers in RGD have been used to annotate
NF2
An association has been curated linking
NF2
and
vestibular schwannomatosis
in Chlorocebus sabaeus.
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
NF2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
25
RGD objects have been annotated to
vestibular schwannomatosis
(DOID:0111252)
0
papers in RGD have been used to annotate
NF2
Curation Notes: ClinVar Annotator: match by term: Neurofibromatosis, type 2
Original References(s):
PMID:10220142
PMID:10691417
PMID:10712203
PMID:10777666
PMID:10970839
PMID:11085592
PMID:11129337
PMID:11448944
PMID:11535133
PMID:11668501
PMID:11756419
PMID:11779178
PMID:11809806
PMID:12118253
PMID:12217955
PMID:12566519
PMID:12695331
PMID:12807969
PMID:1479598
PMID:15598747
PMID:15609345
PMID:15635074
PMID:15645494
PMID:15684865
PMID:15692946
PMID:16199547
PMID:16509493
PMID:16532029
PMID:16983642
PMID:17222329
PMID:17330926
PMID:17576681
PMID:17607601
PMID:18033041
PMID:18173316
PMID:18554169
PMID:18670066
PMID:18766994
PMID:19234911
PMID:19249154
PMID:19451225
PMID:19924781
PMID:19968670
PMID:20553997
PMID:20831745
PMID:21294614
PMID:21563229
PMID:21671232
PMID:21906157
PMID:22012890
PMID:22081132
PMID:22295085
PMID:22325036
PMID:22703879
PMID:22711605
PMID:23196945
PMID:23348505
PMID:23354516
PMID:23921927
PMID:24030433
PMID:24033266
PMID:24309211
PMID:24595234
PMID:24728327
PMID:24815379
PMID:25326635
PMID:2543905
PMID:25525159
PMID:25567352
PMID:25640679
PMID:25741868
PMID:25798586
PMID:25893302
PMID:25931164
PMID:26031996
PMID:26045165
PMID:26066488
PMID:26073919
PMID:26332594
PMID:26343386
PMID:26407091
PMID:26467025
PMID:27128293
PMID:27600092
PMID:27704245
PMID:27854218
PMID:27930734
PMID:28365909
PMID:28492532
PMID:28526081
PMID:28737257
PMID:28873162
PMID:29316957
PMID:29409008
PMID:29489754
PMID:29625052
PMID:29641532
PMID:29685074
PMID:29761250
PMID:29781505
PMID:30306255
PMID:30594554
PMID:30833958
PMID:31089872
PMID:31273341
PMID:31370276
PMID:31712784
PMID:32191290
PMID:32373528
PMID:32724039
PMID:33058421
PMID:33067351
PMID:3313277
PMID:33606809
PMID:35264596
PMID:35449021
PMID:4000972
PMID:7535084
PMID:7666400
PMID:7711726
PMID:7759081
PMID:7868131
PMID:7913580
PMID:7951231
PMID:8012353
PMID:8081368
PMID:8230593
PMID:8379998
PMID:8566958
PMID:8698340
PMID:8751853
PMID:8755919
PMID:8757035
PMID:8797533
PMID:8882871
PMID:8889506
PMID:9391890
PMID:9425229
PMID:9430655
PMID:9466988
PMID:9536098
PMID:9605590
PMID:9643284
PMID:9718334
PMID:9817921
PMID:9817927
PMID:9884492
PMID:9931334
Go Back to source page
Continue to Ontology report