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Browse result for complex cortical dysplasia with other brain malformations

※ introduction

    A brain disease characterized by aberrant neuronal migration and disturbed axonal guidance resulting in variable brain malformations.

Reference
DiseaseOntology: complex cortical dysplasia with other brain malformations


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00677Q1350910381
TUBB3
Tubulin beta-3 chain
Homo sapiens
PTMD02837O602823800
KIF5C
Kinesin heavy chain isoform 5C
Homo sapiens
PTMD03833P0743720306
TUBB
Tubulin beta chain
Homo sapiens
PTMD04554P232587283
TUBG1
Tubulin gamma-1 chain
Homo sapiens
PTMD06641Q138857280
TUBB2A
Tubulin beta-2A chain
Homo sapiens
PTMD06708Q142041778
DYNC1H1
Cytoplasmic dynein 1 heavy chain 1
Homo sapiens
PTMD12185Q9BVA134773
TUBB2B
Tubulin beta-2B chain
Homo sapiens
PTMD14394Q9ULI426153
KIF26A
Kinesin-like protein KIF26A
Homo sapiens
PTMD15017Q9Y6539289
ADGRG1
Adhesion G-protein coupled receptor G1 [Cleaved into: ADGRG1 N-terminal fragment ) ; ADGRG1 C-terminal fragment ) ]
Homo sapiens