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GENE - TERM ANNOTATION REPORT

RGD ID: 14240609
Species: Sus scrofa
RGD Object: Gene
Symbol: LAMA2
Name: laminin subunit alpha 2
Acc ID: DOID:0080918
Term: polymicrogyria
Definition: A brain disease that is characterized by malformation of the developing brain characterized by abnormal cortical lamination and an unusual folding pattern of the cerebral cortex such that all or part of the brain surface is taken up by an excessive number of small folds (gyri). (DO)
Definition Source(s): https://pubmed.ncbi.nlm.nih.gov/10489031/ "DO" "DO", https://www.ncbi.nlm.nih.gov/books/NBK1329/ "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)
LAMA2 ISOLAMA2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: PolymicrogyriaPMID:20207543 PMID:25741868 PMID:28492532 PMID:29706646
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