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GENE - TERM ANNOTATION REPORT

RGD ID: 1562128
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Abcd1
Name: ATP binding cassette subfamily D member 1
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)
Abcd1 ISOABCD1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10190819 PMID:10227685 PMID:10480364 PMID:10737980 PMID:10980309 PMID:11438993 PMID:11748843 PMID:12175782 PMID:12402273 PMID:14767898 PMID:15192815 PMID:15800013 PMID:15811009 PMID:16087056 PMID:16199547 PMID:16415970 PMID:16949688 PMID:17285533 PMID:17372139 PMID:17542813 PMID:19129531 PMID:19325113 PMID:20661612 PMID:20800589 PMID:20859061 PMID:21068741 PMID:21300044 PMID:21700483 PMID:21889498 PMID:21966424 PMID:22045812 PMID:22189598 PMID:22280810 PMID:22479560 PMID:22483867 PMID:23419472 PMID:23430809 PMID:23566833 PMID:23864971 PMID:24154795 PMID:24719134 PMID:24920594 PMID:25118695 PMID:25275259 PMID:25324868 PMID:25741868 PMID:26227820 PMID:26266984 PMID:26454440 PMID:26467025 PMID:27928321 PMID:28086082 PMID:28216041 PMID:28481932 PMID:28492532 PMID:28708278 PMID:28991658 PMID:29056270 PMID:30069915 PMID:30902905 PMID:31074578 PMID:31104286 PMID:31526374 PMID:32003821 PMID:32047678 PMID:32101828 PMID:33247909 PMID:33920672 PMID:34946879 PMID:35053399 PMID:35076462 PMID:35466195 PMID:37977233 PMID:39825153 PMID:7581394 PMID:7668254 PMID:7717396 PMID:7825602 PMID:7849723 PMID:8535452 PMID:8566952 PMID:8651290 PMID:9088111 PMID:9195223 PMID:9242200 PMID:9425230 PMID:9553942 PMID:9712540 PMID:9846054
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