Schizencephaly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The presence of a cleft in the cerebral cortex unilaterally or bilaterally, usually located in the frontal area. (Human Phenotype Ontology, HP_0010636)
External Link https://www.disgenet.org/browser/0/1/0/C0266484
Similar Terms
Downloads & Tools

Genes

10 genes associated with the disease Schizencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
COL4A1 collagen, type IV, alpha 1
COL4A2 collagen, type IV, alpha 2
EMX2 empty spiracles homeobox 2
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
SHH sonic hedgehog
SIX3 SIX homeobox 3
SOX2 SRY (sex determining region Y)-box 2
TUBB2B tubulin, beta 2B class IIb
WDR62 WD repeat domain 62
WNT1 wingless-type MMTV integration site family, member 1