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
RGD ID:
621114
Species:
Rattus norvegicus
RGD Object:
Gene
Symbol:
Ttn
Name:
titin
Acc ID:
DOID:0110315
Term:
hypertrophic cardiomyopathy 9
Definition:
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TTN gene on chromosome 2q31. (DO)
Definition Source(s):
https://www.ncbi.nlm.nih.gov/pubmed/10462489
"DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object Symbol
Qualifier
Evidence
With
Reference
Source
Notes
Original Reference(s)
Ttn
ISO
TTN (Homo sapiens)
7240710
OMIM
Ttn
ISO
TTN (Homo sapiens)
11554173
CTD
CTD Direct Evidence: marker/mechanism
PMID:10462489
PMID:22335739
Ttn
ISO
TTN (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Familial hypertrophic cardiomyopathy 9 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 9
PMID:10462489
PMID:11310621
PMID:16084088
PMID:17344846
PMID:17576681
PMID:18414213
PMID:18948003
PMID:21810661
PMID:22335739
PMID:22526018
PMID:22577215
PMID:22577218
PMID:22577220
PMID:23396983
PMID:23418287
PMID:23446887
PMID:23486992
PMID:23514108
PMID:23606733
PMID:23620651
PMID:23675308
PMID:23852418
PMID:23861362
PMID:23975875
PMID:23995273
PMID:24033266
PMID:24082139
PMID:24119082
PMID:24231549
PMID:24384345
PMID:24395473
PMID:24444549
PMID:24459294
PMID:24503780
PMID:24558114
PMID:24575448
PMID:24636144
PMID:24884718
PMID:24980681
PMID:25037085
PMID:25214167
PMID:25253871
PMID:25326635
PMID:25332820
PMID:25448463
PMID:25500009
PMID:25589632
PMID:25741868
PMID:25741905
PMID:25825243
PMID:25987458
PMID:26269091
PMID:26272908
PMID:26383259
PMID:26467025
PMID:26473617
PMID:26498160
PMID:26516846
PMID:26518445
PMID:26567375
PMID:26597493
PMID:26627873
PMID:26701604
PMID:26718681
PMID:26735901
PMID:26777568
PMID:27066551
PMID:27302369
PMID:27437900
PMID:27437901
PMID:27493940
PMID:27532257
PMID:27796757
PMID:27854229
PMID:27869827
PMID:27930701
PMID:27959697
PMID:28045975
PMID:28166282
PMID:28256728
PMID:28295036
PMID:28333919
PMID:28416588
PMID:28492532
PMID:28611029
PMID:28716623
PMID:28750076
PMID:28771489
PMID:28798025
PMID:28822653
PMID:29420653
PMID:29435569
PMID:29447731
PMID:29511324
PMID:29540445
PMID:29590070
PMID:29691892
PMID:29892087
PMID:29956481
PMID:29961767
PMID:29988065
PMID:30021846
PMID:30086531
PMID:30109841
PMID:30238059
PMID:30371277
PMID:30453078
PMID:30535219
PMID:30536954
PMID:30571272
PMID:30609409
PMID:30615648
PMID:30847666
PMID:31112426
PMID:31127727
PMID:31215789
PMID:31251381
PMID:31395899
PMID:31407473
PMID:31514951
PMID:31561939
PMID:31589614
PMID:31660661
PMID:31737537
PMID:31931689
PMID:31980526
PMID:31983221
PMID:32039858
PMID:32160020
PMID:32235935
PMID:32277046
PMID:32403337
PMID:32528171
PMID:32746448
PMID:32778822
PMID:32880476
PMID:32901917
PMID:32964742
PMID:33106378
PMID:33226272
PMID:33432171
PMID:33449170
PMID:33500567
PMID:33552729
PMID:33874732
PMID:33906374
PMID:34036930
PMID:34106991
PMID:34135346
PMID:34315225
PMID:34495297
PMID:34540771
PMID:34782754
PMID:34935411
PMID:35081925
PMID:35177841
PMID:35207729
PMID:35628876
PMID:35629941
PMID:35653365
PMID:35741838
PMID:36264615
PMID:9536098
Go Back to source page
Continue to Ontology report