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GENE - TERM ANNOTATION REPORT

RGD ID: 1607082
Species: Homo sapiens
RGD Object: Gene
Symbol: TUBA1A
Name: tubulin alpha 1a
Acc ID: DOID:9004667
Term: Malformations of Cortical Development, Group II
Definition: Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICULAR NODULAR HETEROTOPIA.
Definition Source(s): MESH:D054081
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)
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