Welcome
Sign In
Message Center
1 Messages
Go to Message Center
Watched Genes
Watched Ontology Terms
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
Subscribe to Updates
Select categories you would like to watch. Updates to this gene will be sent to Sign In
Analyze List
×
Gene Annotator (Functional Annotation)
unavailable
Gene Annotator (Annotation Distribution)
unavailable
Variant Visualizer (Genomic Variants)
unavailable
InterViewer (Protein-Protein Interactions)
unavailable
Gviewer (Genome Viewer)
unavailable
Variant Visualizer (Damaging Variants)
unavailable
Gene Annotator (Annotation Comparison)
unavailable
OLGA (Gene List Generator)
unavailable
Excel (Download)
MOET (Multi-Ontology Enrichement)
unavailable
GOLF (Gene-Ortholog Location Finder)
unavailable
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
1 Annotations Found.
An association has been curated linking
NPHS2
and
nephrotic syndrome type 1
in Sus scrofa.
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
NPHS2 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
14
RGD objects have been annotated to
nephrotic syndrome type 1
(DOID:0080390)
0
papers in RGD have been used to annotate
NPHS2
Curation Notes: ClinVar Annotator: match by term: Congenital nephrotic syndrome 1 | ClinVar Annotator: match by term: Finnish congenital nephrotic syndrome | ClinVar Annotator: match by term: Idiopathic nephrotic syndrome
Original References(s):
PMID:10742096
PMID:11729243
PMID:11805166
PMID:11805168
PMID:12464671
PMID:12644922
PMID:12707396
PMID:12776285
PMID:14570703
PMID:14675423
PMID:14701729
PMID:14978175
PMID:15042551
PMID:15059485
PMID:15253708
PMID:15264208
PMID:15322893
PMID:15496146
PMID:15769810
PMID:15817495
PMID:15954915
PMID:16286890
PMID:16291839
PMID:16354237
PMID:16721582
PMID:16810518
PMID:16898497
PMID:16900088
PMID:17109732
PMID:17699384
PMID:17899208
PMID:17942957
PMID:18216321
PMID:18683072
PMID:18823551
PMID:19067903
PMID:19145239
PMID:19371226
PMID:19406966
PMID:19674119
PMID:19812541
PMID:19876656
PMID:20333530
PMID:20507940
PMID:20798252
PMID:20947785
PMID:21355056
PMID:21415313
PMID:22578956
PMID:23013956
PMID:23349334
PMID:23515051
PMID:23595123
PMID:23645318
PMID:24033266
PMID:24072147
PMID:24227627
PMID:24509478
PMID:24742477
PMID:25349199
PMID:25525159
PMID:25720465
PMID:25741868
PMID:26211502
PMID:26413278
PMID:26420286
PMID:26455708
PMID:26467025
PMID:26467726
PMID:27885584
PMID:28385484
PMID:28492532
PMID:28658201
PMID:28712774
PMID:28780565
PMID:29382718
PMID:29644057
PMID:29660491
PMID:29982877
PMID:30013592
PMID:30348286
PMID:30609409
PMID:30655312
PMID:32129207
PMID:32581362
PMID:32604935
PMID:33102883
PMID:33305316
PMID:33532864
PMID:8589695
Go Back to source page
Continue to Ontology report