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:
731392
Species:
Homo sapiens
RGD Object:
Gene
Symbol:
ATP7B
Name:
ATPase copper transporting beta
Acc ID:
DOID:630
Term:
genetic disease
Definition:
A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s):
http://ghr.nlm.nih.gov/
"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)
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:19371217
PMID:22677543
PMID:23518715
PMID:24094725
PMID:25741868
PMID:28492532
PMID:9311736
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11690702
PMID:16649058
PMID:16696937
PMID:17717039
PMID:18034201
PMID:22240481
PMID:23235335
PMID:23843956
PMID:25741868
PMID:27022412
PMID:28492532
PMID:9199563
PMID:9671269
PMID:9829905
PMID:9837819
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10453196
PMID:10790207
PMID:15967699
PMID:17576681
PMID:17587212
PMID:18203200
PMID:18371106
PMID:20453399
PMID:20491539
PMID:22484412
PMID:22692182
PMID:23556051
PMID:24010089
PMID:24253677
PMID:25130000
PMID:25741868
PMID:26269689
PMID:28492532
PMID:29930488
PMID:9452121
PMID:9536098
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:10544227
PMID:16283883
PMID:17317524
PMID:17949296
PMID:23518715
PMID:25741868
PMID:27398169
PMID:28492532
PMID:7626145
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:23518715
PMID:23525077
PMID:25741868
PMID:27022412
PMID:27528516
PMID:27982432
PMID:28492532
PMID:33719328
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:18483695
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:1000228
PMID:18373411
PMID:20465995
PMID:22692182
PMID:23389864
PMID:24033266
PMID:25741868
PMID:28492532
PMID:28554332
PMID:29790872
PMID:30097039
PMID:30556376
PMID:30702195
PMID:31059521
PMID:32248359
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10502777
PMID:10544227
PMID:15024742
PMID:15952988
PMID:17264425
PMID:17634212
PMID:17823867
PMID:22692182
PMID:24094725
PMID:24661374
PMID:25741868
PMID:25982861
PMID:27982432
PMID:28492532
PMID:30120852
PMID:30212743
PMID:30655162
PMID:31059521
PMID:32778786
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:18373411
PMID:20465995
PMID:22692182
PMID:23235335
PMID:24253677
PMID:25741868
PMID:27935710
PMID:28492532
PMID:30097039
PMID:31059521
PMID:31449670
PMID:31751128
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:23518715
PMID:28492532
PMID:36096368
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:11405812
PMID:16088907
PMID:16283883
PMID:18034201
PMID:20931554
PMID:21796144
PMID:24146181
PMID:25741868
PMID:26483271
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:15205462
PMID:15723329
PMID:16175588
PMID:17272994
PMID:17717039
PMID:21398519
PMID:22692182
PMID:23518715
PMID:24033266
PMID:25741868
PMID:2610069
PMID:26483271
PMID:28492532
PMID:33640437
PMID:35245129
PMID:36096368
PMID:9311736
PMID:9482578
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:23518715
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:15967699
PMID:16088907
PMID:17919502
PMID:18371106
PMID:22677543
PMID:23518715
PMID:24706876
PMID:25741868
PMID:28492532
PMID:30097039
PMID:30232804
PMID:31449670
PMID:32248359
PMID:34400371
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:16088907
PMID:22692182
PMID:23518715
PMID:24253677
PMID:26206375
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:27398169
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:10502776
PMID:10502777
PMID:10544227
PMID:11216666
PMID:11690702
PMID:12557139
PMID:12885331
PMID:12955875
PMID:15024742
PMID:15952988
PMID:16133174
PMID:16283883
PMID:16791614
PMID:18034201
PMID:19118915
PMID:20517649
PMID:21219664
PMID:21796144
PMID:22735241
PMID:23159873
PMID:23982005
PMID:24897373
PMID:25390358
PMID:25741868
PMID:26253413
PMID:26799313
PMID:28212618
PMID:28492532
PMID:30884209
PMID:7626145
PMID:8533760
PMID:9199563
PMID:9311736
PMID:9504786
PMID:9801873
PMID:9829905
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10502776
PMID:10502777
PMID:10790207
PMID:11405812
PMID:15967699
PMID:16207219
PMID:16283883
PMID:17154398
PMID:17160357
PMID:17272994
PMID:17949296
PMID:19937698
PMID:20517649
PMID:20931554
PMID:20958917
PMID:21682854
PMID:21796144
PMID:22677543
PMID:22692182
PMID:23333878
PMID:2333878
PMID:23518715
PMID:23567103
PMID:25741868
PMID:27022412
PMID:28271598
PMID:28492532
PMID:8782057
PMID:9311736
PMID:9671269
PMID:9801873
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10502777
PMID:20333758
PMID:22692182
PMID:23518715
PMID:25741868
PMID:28492532
PMID:34470610
PMID:35220961
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
PMID:30556376
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:17576681
PMID:25497208
PMID:25617204
PMID:25741868
PMID:28492532
PMID:36096368
PMID:9536098
PMID:9671269
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:19062534
PMID:23333878
PMID:25390358
PMID:25741868
PMID:26004889
PMID:28492532
PMID:28717664
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:16283883
PMID:16603785
PMID:19118915
PMID:23159873
PMID:23982005
PMID:25704634
PMID:25741868
PMID:26799313
PMID:26819605
PMID:28492532
PMID:8533760
PMID:9554743
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:17576681
PMID:18373411
PMID:25525159
PMID:25741868
PMID:28492532
PMID:9536098
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:17587212
PMID:22692182
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:15024742
PMID:16199547
PMID:16283883
PMID:17587212
PMID:21796144
PMID:24146181
PMID:25741868
PMID:28492532
PMID:9671269
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
PMID:30254379
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:23518715
PMID:25741868
PMID:28492532
PMID:31620489
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:15952988
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:23843956
PMID:27398169
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:11243728
PMID:15523622
PMID:16283883
PMID:22484412
PMID:23333878
PMID:25617204
PMID:25741868
PMID:28492532
PMID:7626145
PMID:9801873
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:23551039
PMID:25741868
PMID:28492532
PMID:30702195
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:16283883
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:27022412
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
PMID:28515472
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11405812
PMID:23235335
PMID:24878384
PMID:25741868
PMID:27022412
PMID:27706781
PMID:27982432
PMID:28492532
PMID:29063292
PMID:9829905
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:16283883
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:22692182
PMID:23518715
PMID:25678388
PMID:25741868
PMID:28492532
PMID:32770663
PMID:33223529
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:17717039
PMID:17949296
PMID:25741868
PMID:28492532
PMID:31708252
PMID:35041927
PMID:9311736
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10051024
PMID:10406672
PMID:10544227
PMID:11690702
PMID:11857545
PMID:12557139
PMID:15205462
PMID:15523622
PMID:15967699
PMID:16207219
PMID:17717039
PMID:18311837
PMID:18692069
PMID:19306278
PMID:19937698
PMID:20301685
PMID:21398519
PMID:21645214
PMID:22221592
PMID:22240481
PMID:22286624
PMID:22308153
PMID:22692182
PMID:22720308
PMID:22730635
PMID:23430908
PMID:24033266
PMID:24253677
PMID:24897373
PMID:24909901
PMID:25333069
PMID:25741868
PMID:26286547
PMID:28119449
PMID:28492532
PMID:28602929
PMID:28776642
PMID:29674751
PMID:30026388
PMID:30609409
PMID:31589614
PMID:31664448
PMID:31708252
PMID:31980526
PMID:32043565
PMID:32270360
PMID:32532207
PMID:33098801
PMID:33100332
PMID:7626145
PMID:8298641
PMID:8533760
PMID:9214248
PMID:9352458
PMID:9654149
PMID:9724794
PMID:9887381
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10453196
PMID:10721669
PMID:10942420
PMID:11243728
PMID:11405812
PMID:11479773
PMID:12544487
PMID:12812649
PMID:14986826
PMID:16998622
PMID:17160357
PMID:17587212
PMID:18652531
PMID:19419418
PMID:19783880
PMID:19937698
PMID:20301685
PMID:21219664
PMID:21796144
PMID:22692182
PMID:23235335
PMID:23518715
PMID:23843956
PMID:24146181
PMID:24253677
PMID:24878384
PMID:25086856
PMID:25741868
PMID:25988284
PMID:26032686
PMID:26829729
PMID:27398169
PMID:28212618
PMID:28492532
PMID:29181760
PMID:29907136
PMID:29961769
PMID:29979436
PMID:30275481
PMID:30366773
PMID:30384382
PMID:30558096
PMID:30655162
PMID:31010795
PMID:31474638
PMID:31637888
PMID:31743419
PMID:31783295
PMID:31804371
PMID:32794656
PMID:32911910
PMID:33668890
PMID:33763395
PMID:7626145
PMID:9554743
PMID:9837819
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10790207
PMID:12544487
PMID:15024742
PMID:17587212
PMID:18414213
PMID:18483695
PMID:19419418
PMID:20485189
PMID:20931554
PMID:22240481
PMID:22692182
PMID:23235335
PMID:23518715
PMID:25637381
PMID:25741868
PMID:25982861
PMID:26269689
PMID:27398169
PMID:28492532
PMID:7626145
PMID:8298641
PMID:9311736
PMID:9452121
PMID:9654149
PMID:9829905
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11093740
PMID:15024742
PMID:15952988
PMID:15994426
PMID:16233999
PMID:17300695
PMID:17433323
PMID:17919502
PMID:17949296
PMID:18414213
PMID:19118915
PMID:20301685
PMID:20967755
PMID:21832955
PMID:22240481
PMID:22484412
PMID:22692182
PMID:23518715
PMID:23962630
PMID:24253677
PMID:24706876
PMID:25741868
PMID:28492532
PMID:32043565
PMID:32284880
PMID:33159804
PMID:9311736
PMID:9482578
PMID:9671269
PMID:9671279
PMID:9801873
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10447265
PMID:14986826
PMID:15523622
PMID:15845031
PMID:15967699
PMID:18034201
PMID:18371106
PMID:18483695
PMID:20333758
PMID:21034864
PMID:21796144
PMID:23843956
PMID:25089800
PMID:25741868
PMID:26580967
PMID:27022412
PMID:27398169
PMID:27982432
PMID:28212618
PMID:28492532
PMID:29930488
PMID:9801873
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11175281
PMID:11405812
PMID:18414213
PMID:25741868
PMID:28492532
PMID:7626145
PMID:9311736
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:18414213
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:18373411
PMID:20465995
PMID:21794208
PMID:23235335
PMID:23518715
PMID:24253677
PMID:25637381
PMID:25741868
PMID:28492532
PMID:30097039
PMID:31169307
PMID:32248359
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10502777
PMID:10942420
PMID:11093740
PMID:11405812
PMID:11690702
PMID:12557139
PMID:14986826
PMID:16939419
PMID:17717039
PMID:18371106
PMID:19118915
PMID:20517649
PMID:21610751
PMID:22240481
PMID:22692182
PMID:23518715
PMID:24253677
PMID:25741868
PMID:28492532
PMID:29431110
PMID:31980526
PMID:7626145
PMID:9311736
PMID:9837819
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11405812
PMID:18414213
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
PMID:7626145
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10502777
PMID:11857545
PMID:15967699
PMID:17272994
PMID:18483695
PMID:20517649
PMID:21610751
PMID:21682854
PMID:22692182
PMID:22774841
PMID:23518715
PMID:23551039
PMID:23774950
PMID:25741868
PMID:28492532
PMID:8938442
PMID:9671269
PMID:9837819
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:16088907
PMID:17949296
PMID:20333758
PMID:22692182
PMID:23235335
PMID:23518715
PMID:24253677
PMID:25741868
PMID:26206375
PMID:26275891
PMID:27528516
PMID:28492532
PMID:30254379
PMID:30275481
PMID:30556376
PMID:31059521
PMID:31738409
PMID:31980526
PMID:32248359
PMID:33258288
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10502777
PMID:15952988
PMID:16088907
PMID:17300695
PMID:17823867
PMID:18414213
PMID:25741868
PMID:28492532
PMID:7626145
PMID:8533760
PMID:8938442
PMID:9311736
PMID:9801873
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11175281
PMID:18414213
PMID:25741868
PMID:28492532
PMID:7626145
PMID:8533760
PMID:9887381
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:16088907
PMID:18414213
PMID:25741868
PMID:28492532
PMID:8533760
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:24253677
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:28492532
PMID:9311736
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:10544227
PMID:11472373
PMID:15024742
PMID:15952988
PMID:16283883
PMID:16545904
PMID:17897870
PMID:18034201
PMID:18371106
PMID:18414213
PMID:18483695
PMID:19118915
PMID:20967755
PMID:21682854
PMID:21796144
PMID:23518715
PMID:25741868
PMID:27022412
PMID:28492532
PMID:7626145
PMID:8533760
PMID:893844
PMID:8938442
PMID:9311736
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:18855987
PMID:21454443
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10544227
PMID:14962673
PMID:17823867
PMID:18414213
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:23518715
PMID:24253677
PMID:25741868
PMID:28492532
PMID:33869661
PMID:34620762
PMID:35637795
PMID:36632541
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11405812
PMID:14966923
PMID:18034201
PMID:18414213
PMID:22308153
PMID:23235335
PMID:24878384
PMID:25741868
PMID:27398169
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10544227
PMID:16696937
PMID:20045993
PMID:21219664
PMID:22484412
PMID:22692182
PMID:22940187
PMID:25741868
PMID:26483271
PMID:27022412
PMID:27398169
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10441329
PMID:11690702
PMID:15202786
PMID:15967699
PMID:16283883
PMID:21610751
PMID:23982005
PMID:25741868
PMID:28492532
PMID:34470610
PMID:8938442
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:15024742
PMID:17919502
PMID:19033537
PMID:20437613
PMID:21454443
PMID:22106832
PMID:22677543
PMID:22820477
PMID:22898812
PMID:23518715
PMID:25741868
PMID:28492532
PMID:28564725
PMID:29063292
PMID:29473088
PMID:30097039
PMID:30275481
PMID:30723317
PMID:31408533
PMID:31589614
PMID:32248359
PMID:32770663
PMID:33640437
PMID:34426522
PMID:36096368
PMID:626829
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10447265
PMID:18414213
PMID:20517649
PMID:22484412
PMID:22677543
PMID:22692182
PMID:23518715
PMID:24517292
PMID:25741868
PMID:25825851
PMID:26764160
PMID:28492532
PMID:30097039
PMID:30232804
PMID:32043565
PMID:32118851
PMID:32154060
PMID:32248359
PMID:33640437
PMID:34620762
PMID:36573661
PMID:9671269
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10502777
PMID:15337266
PMID:15967699
PMID:18371106
PMID:18414213
PMID:23518715
PMID:24023303
PMID:25741868
PMID:28492532
PMID:9671269
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:11021476
PMID:11093740
PMID:15952988
PMID:16922724
PMID:17433323
PMID:17949296
PMID:18371106
PMID:18414213
PMID:21350584
PMID:22692182
PMID:23158531
PMID:23219664
PMID:23518715
PMID:23843956
PMID:24033266
PMID:24094725
PMID:25741868
PMID:27022412
PMID:27398169
PMID:28492532
PMID:28554332
PMID:30254379
PMID:30275481
PMID:30702195
PMID:31980526
PMID:32248359
PMID:33159804
PMID:33258288
PMID:34470610
PMID:34620762
PMID:35245129
PMID:35470480
PMID:35637795
PMID:9311736
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:14962673
PMID:16088907
PMID:16472602
PMID:17680703
PMID:21454443
PMID:23430806
PMID:24253677
PMID:25741868
PMID:28492532
PMID:30842500
PMID:31751128
PMID:32248359
PMID:32685348
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:10544227
PMID:16207219
PMID:17919502
PMID:18203200
PMID:18371106
PMID:22240481
PMID:22677543
PMID:22735241
PMID:23518715
PMID:24706876
PMID:25741868
PMID:26799313
PMID:28492532
PMID:29063292
PMID:31598802
PMID:33640437
PMID:34400371
PMID:36096368
PMID:8533760
PMID:8938442
PMID:9311736
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:18414213
PMID:25741868
PMID:28492532
ATP7B
IAGP
(Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Inborn genetic diseases
PMID:18414213
PMID:25741868
PMID:28492532
Go Back to source page
Continue to Ontology report