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GENE - TERM ANNOTATION REPORT

RGD ID: 1309427
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Tubb2b
Name: tubulin, beta 2B class IIb
Acc ID: DOID:0050453
Term: lissencephaly
Definition: A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Lissencephaly "DO" "DO", http://www.ninds.nih.gov/disorders/lissencephaly/lissencephaly.htm "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)
Tubb2b ISOTUBB2B (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: LissencephalyPMID:11425694 PMID:23001566 PMID:25741868 PMID:29671837
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