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
Tmprss3
and
autosomal recessive nonsyndromic deafness 8
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
TMPRSS3 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
autosomal recessive nonsyndromic deafness 8
(DOID:0110527)
0
papers in RGD have been used to annotate
Tmprss3
An association has been curated linking
Tmprss3
and
autosomal recessive nonsyndromic deafness 8
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
TMPRSS3 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
1
RGD objects have been annotated to
autosomal recessive nonsyndromic deafness 8
(DOID:0110527)
0
papers in RGD have been used to annotate
Tmprss3
Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 10 | ClinVar Annotator: match by term: Deafness, autosomal recessive 8 | ClinVar Annotator: match by term: NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 8
Original References(s):
PMID:11137999
PMID:11424922
PMID:11462234
PMID:11907649
PMID:12393794
PMID:12920079
PMID:15447792
PMID:16021470
PMID:16283880
PMID:16460646
PMID:16524950
PMID:17551081
PMID:17576681
PMID:19170735
PMID:21534946
PMID:21786053
PMID:22382023
PMID:22975204
PMID:23208854
PMID:23958653
PMID:23967202
PMID:24033266
PMID:24416283
PMID:24526180
PMID:24657061
PMID:24853665
PMID:25262649
PMID:25474651
PMID:25741868
PMID:25770132
PMID:26036852
PMID:26346818
PMID:26408194
PMID:26445815
PMID:26467025
PMID:26969326
PMID:27344577
PMID:28246597
PMID:28263784
PMID:28492532
PMID:28566687
PMID:28695016
PMID:28984810
PMID:29196752
PMID:29293505
PMID:29431110
PMID:29889784
PMID:30242206
PMID:30303587
PMID:30311386
PMID:30622556
PMID:31045651
PMID:31053783
PMID:31152317
PMID:31412945
PMID:31581539
PMID:31589614
PMID:31980526
PMID:32235586
PMID:32306631
PMID:3285355
PMID:32853555
PMID:32860223
PMID:34416374
PMID:34440452
PMID:34599368
PMID:34868270
PMID:35802133
PMID:35864128
PMID:36633841
PMID:9536098
Go Back to source page
Continue to Ontology report