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
Vps13b
and
Cohen syndrome
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
VPS13B (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
36
RGD objects have been annotated to
Cohen syndrome
(DOID:0111590)
0
papers in RGD have been used to annotate
Vps13b
An association has been curated linking
Vps13b
and
Cohen syndrome
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
VPS13B (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
36
RGD objects have been annotated to
Cohen syndrome
(DOID:0111590)
0
papers in RGD have been used to annotate
Vps13b
Curation Notes: ClinVar Annotator: match by term: Cohen syndrome | ClinVar Annotator: match by term: VPS13B-related condition
Original References(s):
PMID:11169562
PMID:12730828
PMID:15141358
PMID:15154116
PMID:15173253
PMID:15211651
PMID:15498460
PMID:15691367
PMID:15918062
PMID:16199547
PMID:16648375
PMID:16917849
PMID:17383910
PMID:17576681
PMID:17786118
PMID:17990063
PMID:18414213
PMID:18655112
PMID:19006247
PMID:19190672
PMID:19533689
PMID:19763152
PMID:20307669
PMID:20461111
PMID:20656880
PMID:20683995
PMID:20921020
PMID:21330571
PMID:21659346
PMID:21865173
PMID:22382802
PMID:22406018
PMID:22527104
PMID:22700954
PMID:22855652
PMID:23033978
PMID:23188044
PMID:23352163
PMID:23757202
PMID:24033266
PMID:24311531
PMID:24334746
PMID:24334764
PMID:25060287
PMID:25326635
PMID:25356970
PMID:25472526
PMID:25502226
PMID:25525159
PMID:25533962
PMID:25640679
PMID:25741868
PMID:25741914
PMID:25741915
PMID:25741916
PMID:26104215
PMID:26133662
PMID:26395554
PMID:26443248
PMID:26467025
PMID:26539891
PMID:26938784
PMID:27175599
PMID:27353947
PMID:27380831
PMID:27533158
PMID:27829003
PMID:28041643
PMID:28057753
PMID:28341476
PMID:28492532
PMID:28559085
PMID:28631888
PMID:28832562
PMID:29149870
PMID:29431110
PMID:29453417
PMID:29634382
PMID:29706646
PMID:29758347
PMID:30138938
PMID:30290665
PMID:30792901
PMID:30843084
PMID:31444703
PMID:31580008
PMID:31736247
PMID:31943017
PMID:31965297
PMID:32170714
PMID:32384097
PMID:32483926
PMID:32505691
PMID:32581362
PMID:32860008
PMID:32919079
PMID:32959227
PMID:33023636
PMID:33025479
PMID:33217554
PMID:33994118
PMID:34006472
PMID:34353225
PMID:34425733
PMID:35690661
PMID:9536098
Go Back to source page
Continue to Ontology report