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GENE - TERM ANNOTATION REPORT

RGD ID: 18341127
Species: Chlorocebus sabaeus
RGD Object: Gene
Symbol: FMO3
Name: flavin containing dimethylaniline monoxygenase 3
Acc ID: DOID:0080361
Term: trimethylaminuria
Definition: An inherited metabolic disorder characterized by the inabilty to break down trimethylamine and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding flavin-containing monooxygenase-3 on chromosome 1q24. (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/trimethylaminuria "DO" "DO", https://www.genome.gov/Genetic-Disorders/Trimethylaminuria "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)
FMO3 ISOFMO3 (Homo sapiens)7240710OMIM  
FMO3 ISOFMO3 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: TrimethylaminuriaPMID:10338091 PMID:10376762 PMID:10479479 PMID:10898113 PMID:11136294 PMID:11191884 PMID:11266081 PMID:12228178 PMID:12527699 PMID:12678693 PMID:12814961 PMID:12893987 PMID:12938085 PMID:15203093 PMID:15564885 PMID:15618671 PMID:15618753 PMID:16296944 PMID:16600650 PMID:16601883 PMID:16858129 PMID:16996766 PMID:17096187 PMID:17142560 PMID:17224546 PMID:17329912 PMID:17531949 PMID:17584019 PMID:18028028 PMID:18423897 PMID:19321370 PMID:19577495 PMID:20301282 PMID:21422137 PMID:21451776 PMID:22819296 PMID:23567996 PMID:23791655 PMID:25741868 PMID:25870212 PMID:27118741 PMID:27523475 PMID:28196478 PMID:28392825 PMID:28492532 PMID:28649550 PMID:28743400 PMID:29116146 PMID:29555771 PMID:30351217 PMID:31180159 PMID:31240165 PMID:31401033 PMID:31533761 PMID:31580948 PMID:31589614 PMID:31980526 PMID:32653296 PMID:33473342 PMID:33831674 PMID:34634752 PMID:34834137 PMID:35853340 PMID:37930845 PMID:8401051 PMID:9282831 PMID:9398858 PMID:9536088 PMID:987532
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