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
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
Enpp1
and
Generalized Arterial Calcification of Infancy, 1
in Rattus norvegicus.
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
ENPP1 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
3
RGD objects have been annotated to
Generalized Arterial Calcification of Infancy, 1
(DOID:9006958)
42
papers in RGD have been used to annotate
Enpp1
An association has been curated linking
Enpp1
and
Generalized Arterial Calcification of Infancy, 1
in Rattus norvegicus.
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
ENPP1 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
3
RGD objects have been annotated to
Generalized Arterial Calcification of Infancy, 1
(DOID:9006958)
42
papers in RGD have been used to annotate
Enpp1
Curation Notes: ClinVar Annotator: match by term: Arterial calcification, generalized, of infancy, 1
Original References(s):
PMID:10453738
PMID:10480624
PMID:11159191
PMID:11739459
PMID:11771660
PMID:12881724
PMID:14671192
PMID:14988267
PMID:15001634
PMID:15126519
PMID:15605415
PMID:15677494
PMID:15940697
PMID:16025115
PMID:16315058
PMID:16369898
PMID:16607460
PMID:16609882
PMID:16968801
PMID:17576681
PMID:18950909
PMID:19206175
PMID:19229237
PMID:20016754
PMID:20137773
PMID:20981035
PMID:22209248
PMID:22539483
PMID:23027977
PMID:23041369
PMID:24033266
PMID:25326635
PMID:25741868
PMID:26857895
PMID:27238374
PMID:27467858
PMID:27467859
PMID:28377967
PMID:28492532
PMID:28973083
PMID:29141319
PMID:29244957
PMID:29979387
PMID:31444901
PMID:31805212
PMID:31826312
PMID:32573669
PMID:33005041
PMID:33465815
PMID:34609116
PMID:34633109
PMID:34906475
PMID:35276006
PMID:35475527
PMID:35482848
PMID:35738466
PMID:35854274
PMID:8960499
PMID:9536098
PMID:9662402
Go Back to source page
Continue to Ontology report