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
Behavioral & Substance Use Disorder
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
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
Ntrk1
and
hereditary sensory neuropathy type 4
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
NTRK1 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
4
RGD objects have been annotated to
hereditary sensory neuropathy type 4
(DOID:0070146)
0
papers in RGD have been used to annotate
Ntrk1
An association has been curated linking
Ntrk1
and
hereditary sensory neuropathy type 4
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
NTRK1 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
4
RGD objects have been annotated to
hereditary sensory neuropathy type 4
(DOID:0070146)
0
papers in RGD have been used to annotate
Ntrk1
Curation Notes: ClinVar Annotator: match by term: Hereditary Sensory and Autonomic Neuropathy Type IV | ClinVar Annotator: match by term: NTRK1-related condition | ClinVar Annotator: match by term: hereditary sensory and autonomic neuropathy type 4
Original References(s):
PMID:0233776
PMID:10090906
PMID:10233776
PMID:10330344
PMID:10443680
PMID:10861667
PMID:10982191
PMID:11071380
PMID:11139246
PMID:11159935
PMID:11310631
PMID:11668614
PMID:11719521
PMID:11748840
PMID:12210794
PMID:12406349
PMID:12949319
PMID:15534759
PMID:16199547
PMID:16373086
PMID:17576681
PMID:18056464
PMID:18162686
PMID:18179783
PMID:18322713
PMID:18955016
PMID:19250380
PMID:19598235
PMID:19618435
PMID:19651702
PMID:20003389
PMID:20301726
PMID:20647579
PMID:21708027
PMID:22032467
PMID:22302274
PMID:22397633
PMID:22653642
PMID:22957891
PMID:23112235
PMID:23241418
PMID:23799134
PMID:24088041
PMID:24154508
PMID:24631696
PMID:25359976
PMID:25519000
PMID:25640679
PMID:25741868
PMID:25984678
PMID:26215504
PMID:26467025
PMID:26633545
PMID:26925801
PMID:27058611
PMID:27184211
PMID:27265460
PMID:27544236
PMID:27551041
PMID:27676246
PMID:27698470
PMID:27761255
PMID:28177573
PMID:28192073
PMID:28328124
PMID:28345382
PMID:28492532
PMID:28940190
PMID:28981924
PMID:29190530
PMID:29619836
PMID:29770739
PMID:30002500
PMID:30201336
PMID:30774415
PMID:31069529
PMID:31130284
PMID:32214227
PMID:32219930
PMID:32369273
PMID:32707200
PMID:32707409
PMID:32807182
PMID:32901917
PMID:33235206
PMID:33422294
PMID:33748046
PMID:34193129
PMID:34405299
PMID:34480478
PMID:3472625
PMID:35471943
PMID:37248554
PMID:38581121
PMID:77656
PMID:8696348
PMID:9536098
Go Back to source page
Continue to Ontology report