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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 SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:19371217 PMID:22677543 PMID:23518715 PMID:24094725 PMID:25741868 PMID:28492532 PMID:9311736
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10441329 PMID:10544227 PMID:16283883 PMID:17317524 PMID:17949296 PMID:23518715 PMID:25741868 PMID:27398169 PMID:28492532 PMID:7626145
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:23518715 PMID:23525077 PMID:25741868 PMID:27022412 PMID:27528516 PMID:27982432 PMID:28492532 PMID:33719328
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:18483695 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:23518715 PMID:28492532 PMID:36096368
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:23518715 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:16088907 PMID:22692182 PMID:23518715 PMID:24253677 PMID:26206375
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:27398169 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10502777 PMID:20333758 PMID:22692182 PMID:23518715 PMID:25741868 PMID:28492532 PMID:34470610 PMID:35220961
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532 PMID:30556376
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:17576681 PMID:25497208 PMID:25617204 PMID:25741868 PMID:28492532 PMID:36096368 PMID:9536098 PMID:9671269
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:19062534 PMID:23333878 PMID:25390358 PMID:25741868 PMID:26004889 PMID:28492532 PMID:28717664
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:17576681 PMID:18373411 PMID:25525159 PMID:25741868 PMID:28492532 PMID:9536098
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:17587212 PMID:22692182 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10441329 PMID:15024742 PMID:16199547 PMID:16283883 PMID:17587212 PMID:21796144 PMID:24146181 PMID:25741868 PMID:28492532 PMID:9671269
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532 PMID:30254379
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:23518715 PMID:25741868 PMID:28492532 PMID:31620489
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:15952988 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:23843956 PMID:27398169 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:23551039 PMID:25741868 PMID:28492532 PMID:30702195
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10441329 PMID:16283883 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:27022412
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532 PMID:28515472
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11405812 PMID:23235335 PMID:24878384 PMID:25741868 PMID:27022412 PMID:27706781 PMID:27982432 PMID:28492532 PMID:29063292 PMID:9829905
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10441329 PMID:16283883 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:22692182 PMID:23518715 PMID:25678388 PMID:25741868 PMID:28492532 PMID:32770663 PMID:33223529
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:17717039 PMID:17949296 PMID:25741868 PMID:28492532 PMID:31708252 PMID:35041927 PMID:9311736
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11175281 PMID:11405812 PMID:18414213 PMID:25741868 PMID:28492532 PMID:7626145 PMID:9311736
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:18414213 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11405812 PMID:18414213 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532 PMID:7626145
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11175281 PMID:18414213 PMID:25741868 PMID:28492532 PMID:7626145 PMID:8533760 PMID:9887381
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:16088907 PMID:18414213 PMID:25741868 PMID:28492532 PMID:8533760
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:24253677 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532 PMID:9311736
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:18855987 PMID:21454443 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10544227 PMID:14962673 PMID:17823867 PMID:18414213 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:23518715 PMID:24253677 PMID:25741868 PMID:28492532 PMID:33869661 PMID:34620762 PMID:35637795 PMID:36632541
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11405812 PMID:14966923 PMID:18034201 PMID:18414213 PMID:22308153 PMID:23235335 PMID:24878384 PMID:25741868 PMID:27398169 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10502777 PMID:15337266 PMID:15967699 PMID:18371106 PMID:18414213 PMID:23518715 PMID:24023303 PMID:25741868 PMID:28492532 PMID:9671269
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID: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)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:18414213 PMID:25741868 PMID:28492532
ATP7B IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:18414213 PMID:25741868 PMID:28492532
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