complex cortical dysplasia with other brain malformations 1

Summary
Synonym
  • CDCBM1
  • cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Definition
A complex cortical dysplasia with other brain malformations that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta 3 class III (TUBB3) gene on chromosome 16q24.3.
Super Class
complex cortical dysplasia with other brain malformations
External Links
Disease Ontology
DOID:0090137
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying entries 21 - 26 of 26 in total
Gene ID Gene Symbol Description Source
79147 FKRP fukutin related protein
84197 POMK protein O-mannose kinase
84892 POMGNT2 protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)
148789 B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
160418 TMTC3 transmembrane O-mannosyltransferase targeting cadherins 3
729920 CRPPA CDP-L-ribitol pyrophosphorylase A

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024