# GeDiPNet Cluster 175 -- Top Shared Genes -- generated 2026-10-09 08:25:50
# Curated genes (disease_gdp) linked to 2 or more of this cluster's member diseases, most widely shared first. Data as of: 2026-10-09 03:15:01.
Gene	Member Diseases Linked	Cluster Size	Linked Diseases
TUBB2B	5	8	Complex cortical dysplasia with other brain malformations; Congenital fibrosis of extraocular muscles; Cortical development malformation; Cortical dysplasia with other brain malformations; Tubulinopathy
TUBG1	5	8	15q11.2 microdeletion syndrome; Complex cortical dysplasia with other brain malformations; Cortical development malformation; Cortical dysplasia with other brain malformations; lissencephaly spectrum disorders
TUBB3	4	8	Complex cortical dysplasia with other brain malformations; Congenital fibrosis of extraocular muscles; Cortical dysplasia with other brain malformations; Tubulinopathy
KIF2A	3	8	Complex cortical dysplasia with other brain malformations; Cortical development malformation; Cortical dysplasia with other brain malformations
KIF5C	3	8	Complex cortical dysplasia with other brain malformations; Cortical development malformation; Cortical dysplasia with other brain malformations
TUBA1A	3	8	Congenital fibrosis of extraocular muscles; Cortical development malformation; Tubulinopathy
TUBB	3	8	Complex cortical dysplasia with other brain malformations; Congenital fibrosis of extraocular muscles; Cortical dysplasia with other brain malformations
TUBB2A	3	8	Complex cortical dysplasia with other brain malformations; Cortical dysplasia with other brain malformations; Tubulinopathy
APC2	2	8	Cortical dysplasia with other brain malformations; lissencephaly spectrum disorders
DYNC1H1	2	8	Cortical development malformation; Cortical dysplasia with other brain malformations
HRAS	2	8	Congenital fibrosis of extraocular muscles; Cortical development malformation
KIF26A	2	8	Complex cortical dysplasia with other brain malformations; Cortical dysplasia with other brain malformations
KIFBP	2	8	Cortical development malformation; goldberg-shprintzen syndrome
TUBGCP2	2	8	Cortical development malformation; Cortical dysplasia with other brain malformations