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GENE - TERM ANNOTATION REPORT

RGD ID: 12601199
Species: Ictidomys tridecemlineatus
RGD Object: Gene
Symbol: Maob
Name: monoamine oxidase B
Acc ID: DOID:0060693
Term: Brunner syndrome
Definition: An amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/8211186 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/8503438 "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)
Maob ISOMAOB (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Brunner syndromePMID:17296899 PMID:20340138 PMID:22382802 PMID:28492532 PMID:30452590 PMID:8211186
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