TUBB2B, tubulin beta 2B class IIb, 347733

N. diseases: 82; N. variants: 14
Disease: Congenital absence of part of brain ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266461
Disease: Congenital absence of part of brain
Congenital absence of part of brain 		0.200 Biomarker disease MGD A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse. 23727838 2013