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
4 Annotations Found.
An association has been curated linking
Pcsk9
and
hypobetalipoproteinemia
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
PCSK9 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
10
RGD objects have been annotated to
hypobetalipoproteinemia
(DOID:1390)
0
papers in RGD have been used to annotate
Pcsk9
Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia | ClinVar Annotator: match by term: Hypobetalipoproteinemia
Original References(s):
PMID:11668641
PMID:12175777
PMID:12730697
PMID:14727156
PMID:15358785
PMID:15654334
PMID:15893176
PMID:16183066
PMID:16211558
PMID:16314194
PMID:16424354
PMID:16465619
PMID:16554528
PMID:16571601
PMID:16912035
PMID:17094996
PMID:17140581
PMID:17170371
PMID:17316651
PMID:17380167
PMID:17461796
PMID:17502126
PMID:17765244
PMID:17804797
PMID:17921436
PMID:17971861
PMID:18197702
PMID:18262190
PMID:18266662
PMID:18280815
PMID:18300938
PMID:18354102
PMID:18559913
PMID:18710658
PMID:18799458
PMID:19001363
PMID:19022446
PMID:19081568
PMID:19191301
PMID:19249440
PMID:19351729
PMID:19797716
PMID:19917273
PMID:20006333
PMID:20031607
PMID:20172854
PMID:20579540
PMID:20623344
PMID:20959675
PMID:21943799
PMID:22095935
PMID:22923420
PMID:23105118
PMID:23375686
PMID:23386946
PMID:23663650
PMID:23726366
PMID:23743349
PMID:23935525
PMID:24033266
PMID:24252255
PMID:24278757
PMID:24507774
PMID:24507775
PMID:24785115
PMID:24808179
PMID:25046268
PMID:25278291
PMID:25412415
PMID:25600226
PMID:25741868
PMID:25744035
PMID:25904937
PMID:26020417
PMID:26049403
PMID:26195630
PMID:26269718
PMID:26332594
PMID:26374825
PMID:26467025
PMID:26541928
PMID:26546829
PMID:26633542
PMID:26636822
PMID:26688439
PMID:26802169
PMID:26902539
PMID:26937405
PMID:27135400
PMID:27206942
PMID:27218270
PMID:27280970
PMID:27516387
PMID:27765764
PMID:27919364
PMID:28008010
PMID:28302345
PMID:28323660
PMID:28360401
PMID:28438747
PMID:28492532
PMID:28587771
PMID:28768753
PMID:28777095
PMID:28965616
PMID:28994502
PMID:29083407
PMID:29127338
PMID:29192238
PMID:29259136
PMID:29261184
PMID:29438441
PMID:29459468
PMID:29593013
PMID:29724976
PMID:29728531
PMID:29748315
PMID:29997226
PMID:30146126
PMID:30270359
PMID:30293936
PMID:30710474
PMID:30971288
PMID:31106297
PMID:31491741
PMID:31893465
PMID:31949048
PMID:31980526
PMID:32044282
PMID:32058034
PMID:32719484
PMID:32770674
PMID:33091218
PMID:33147992
PMID:33231818
PMID:33258288
PMID:33269076
PMID:33303402
PMID:33418990
PMID:33533259
PMID:34074024
PMID:34297352
PMID:34341098
PMID:34521694
PMID:34526433
PMID:35047021
PMID:35910211
PMID:35913489
PMID:35929461
PMID:36087353
PMID:36187800
PMID:36834740
PMID:37443404
PMID:37469559
An association has been curated linking
Pcsk9
and
hypobetalipoproteinemia
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
PCSK9 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
10
RGD objects have been annotated to
hypobetalipoproteinemia
(DOID:1390)
0
papers in RGD have been used to annotate
Pcsk9
Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia | ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL | ClinVar Annotator: match by term: Hypobetalipoproteinemia
Original References(s):
PMID:11668641
PMID:12175777
PMID:12730697
PMID:14727156
PMID:15358785
PMID:15654334
PMID:15893176
PMID:16183066
PMID:16211558
PMID:16314194
PMID:16424354
PMID:16465619
PMID:16554528
PMID:16571601
PMID:16912035
PMID:17094996
PMID:17140581
PMID:17170371
PMID:17316651
PMID:17380167
PMID:17461796
PMID:17502126
PMID:17765244
PMID:17804797
PMID:17921436
PMID:17971861
PMID:18197702
PMID:18262190
PMID:18266662
PMID:18300938
PMID:18354102
PMID:18559913
PMID:18710658
PMID:18799458
PMID:19001363
PMID:19022446
PMID:19081568
PMID:19191301
PMID:19249440
PMID:19351729
PMID:19797716
PMID:19917273
PMID:20006333
PMID:20031607
PMID:20172854
PMID:20579540
PMID:20623344
PMID:20959675
PMID:21146822
PMID:21943799
PMID:22095935
PMID:22923420
PMID:23095242
PMID:23105118
PMID:23375686
PMID:23386946
PMID:23663650
PMID:23743349
PMID:23935525
PMID:24033266
PMID:24278757
PMID:24507774
PMID:24507775
PMID:24785115
PMID:24808179
PMID:24859021
PMID:25014035
PMID:25046268
PMID:25278291
PMID:25412415
PMID:25600226
PMID:25741868
PMID:25744035
PMID:25904937
PMID:25962062
PMID:26020417
PMID:26049403
PMID:26195630
PMID:26332594
PMID:26374825
PMID:26467025
PMID:26541928
PMID:26546829
PMID:26632531
PMID:26633542
PMID:26636822
PMID:26688439
PMID:26802169
PMID:26937405
PMID:27135400
PMID:27206942
PMID:27218270
PMID:27280970
PMID:27516387
PMID:27765764
PMID:27919364
PMID:28008010
PMID:28179607
PMID:28302345
PMID:28323660
PMID:28360401
PMID:28438747
PMID:28492532
PMID:28587771
PMID:28768753
PMID:28777095
PMID:28784313
PMID:28965616
PMID:28994502
PMID:29083407
PMID:29127338
PMID:29259136
PMID:29261184
PMID:29438441
PMID:29459468
PMID:29593013
PMID:29724976
PMID:29748315
PMID:29997226
PMID:30241732
PMID:30270359
PMID:30293936
PMID:30971288
PMID:31106297
PMID:31491741
PMID:31949048
PMID:32044282
PMID:32058034
PMID:32719484
PMID:33147992
PMID:33258288
PMID:33269076
PMID:33303402
PMID:33418990
PMID:34074024
PMID:34521694
PMID:34526433
PMID:35910211
PMID:35929461
PMID:36187800
An association has been curated linking
Pcsk9
and
hypobetalipoproteinemia
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
PCSK9 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
10
RGD objects have been annotated to
hypobetalipoproteinemia
(DOID:1390)
0
papers in RGD have been used to annotate
Pcsk9
Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia | ClinVar Annotator: match by term: Hypobetalipoproteinemia
Original References(s):
PMID:11668641
PMID:12175777
PMID:12730697
PMID:14727156
PMID:15358785
PMID:15654334
PMID:15893176
PMID:16183066
PMID:16211558
PMID:16314194
PMID:16424354
PMID:16465619
PMID:16554528
PMID:16571601
PMID:16912035
PMID:17094996
PMID:17140581
PMID:17170371
PMID:17316651
PMID:17380167
PMID:17461796
PMID:17502126
PMID:17765244
PMID:17804797
PMID:17921436
PMID:17971861
PMID:18197702
PMID:18262190
PMID:18266662
PMID:18300938
PMID:18354102
PMID:18559913
PMID:18710658
PMID:18799458
PMID:19001363
PMID:19022446
PMID:19081568
PMID:19191301
PMID:19249440
PMID:19351729
PMID:19797716
PMID:19917273
PMID:20006333
PMID:20031607
PMID:20172854
PMID:20579540
PMID:20623344
PMID:20959675
PMID:21146822
PMID:21943799
PMID:22095935
PMID:22923420
PMID:23095242
PMID:23105118
PMID:23375686
PMID:23386946
PMID:23663650
PMID:23743349
PMID:23935525
PMID:24033266
PMID:24278757
PMID:24507774
PMID:24507775
PMID:24785115
PMID:24808179
PMID:24859021
PMID:25014035
PMID:25046268
PMID:25278291
PMID:25412415
PMID:25600226
PMID:25741868
PMID:25744035
PMID:25904937
PMID:25962062
PMID:26020417
PMID:26049403
PMID:26195630
PMID:26332594
PMID:26374825
PMID:26467025
PMID:26541928
PMID:26546829
PMID:26632531
PMID:26633542
PMID:26636822
PMID:26688439
PMID:26802169
PMID:26937405
PMID:27135400
PMID:27206942
PMID:27218270
PMID:27280970
PMID:27516387
PMID:27765764
PMID:27919364
PMID:28008010
PMID:28179607
PMID:28302345
PMID:28323660
PMID:28360401
PMID:28438747
PMID:28492532
PMID:28587771
PMID:28768753
PMID:28777095
PMID:28784313
PMID:28965616
PMID:28994502
PMID:29083407
PMID:29127338
PMID:29259136
PMID:29261184
PMID:29438441
PMID:29459468
PMID:29593013
PMID:29724976
PMID:29748315
PMID:29997226
PMID:30241732
PMID:30270359
PMID:30293936
PMID:30971288
PMID:31106297
PMID:31491741
PMID:31949048
PMID:32044282
PMID:32058034
PMID:32719484
PMID:33147992
PMID:33258288
PMID:33269076
PMID:33303402
PMID:33418990
PMID:34074024
PMID:34521694
PMID:34526433
PMID:35929461
An association has been curated linking
Pcsk9
and
hypobetalipoproteinemia
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
PCSK9 (Homo sapiens)
[(IAGP) inferred by association of genotype and phenotype]
10
RGD objects have been annotated to
hypobetalipoproteinemia
(DOID:1390)
0
papers in RGD have been used to annotate
Pcsk9
Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia | ClinVar Annotator: match by term: Hypobetalipoproteinemia
Original References(s):
PMID:11668641
PMID:12175777
PMID:12730697
PMID:14727156
PMID:15358785
PMID:15654334
PMID:15893176
PMID:16183066
PMID:16211558
PMID:16314194
PMID:16424354
PMID:16465619
PMID:16554528
PMID:16571601
PMID:16912035
PMID:17094996
PMID:17140581
PMID:17170371
PMID:17316651
PMID:17380167
PMID:17461796
PMID:17502126
PMID:17765244
PMID:17804797
PMID:17921436
PMID:17971861
PMID:18197702
PMID:18262190
PMID:18266662
PMID:18300938
PMID:18354102
PMID:18559913
PMID:18710658
PMID:18799458
PMID:19001363
PMID:19022446
PMID:19081568
PMID:19191301
PMID:19249440
PMID:19351729
PMID:19797716
PMID:19917273
PMID:20006333
PMID:20031607
PMID:20172854
PMID:20579540
PMID:20623344
PMID:20959675
PMID:21943799
PMID:22095935
PMID:22923420
PMID:23105118
PMID:23375686
PMID:23386946
PMID:23663650
PMID:23743349
PMID:23935525
PMID:24033266
PMID:24278757
PMID:24507774
PMID:24507775
PMID:24785115
PMID:24808179
PMID:25046268
PMID:25278291
PMID:25412415
PMID:25600226
PMID:25741868
PMID:25744035
PMID:25904937
PMID:26020417
PMID:26049403
PMID:26195630
PMID:26332594
PMID:26374825
PMID:26467025
PMID:26541928
PMID:26546829
PMID:26633542
PMID:26636822
PMID:26688439
PMID:26802169
PMID:26937405
PMID:27135400
PMID:27206942
PMID:27218270
PMID:27280970
PMID:27516387
PMID:27765764
PMID:27919364
PMID:28008010
PMID:28302345
PMID:28323660
PMID:28360401
PMID:28438747
PMID:28492532
PMID:28587771
PMID:28768753
PMID:28777095
PMID:28965616
PMID:28994502
PMID:29083407
PMID:29127338
PMID:29259136
PMID:29261184
PMID:29438441
PMID:29459468
PMID:29593013
PMID:29724976
PMID:29748315
PMID:29997226
PMID:30270359
PMID:30293936
PMID:30971288
PMID:31106297
PMID:31491741
PMID:31949048
PMID:32044282
PMID:32058034
PMID:32719484
PMID:33147992
PMID:33258288
PMID:33269076
PMID:33303402
PMID:33418990
PMID:34074024
PMID:34521694
PMID:34526433
PMID:35910211
PMID:35929461
PMID:36187800
Go Back to source page
Continue to Ontology report