Dysgenesis Of Corpus Callosum Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0431369
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Genes

25 genes associated with the disease Dysgenesis Of Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ATG9A autophagy related 9A
CREBBP CREB binding protein
DCHS1 dachsous cadherin-related 1
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
EARS2 glutamyl-tRNA synthetase 2, mitochondrial
EED embryonic ectoderm development
FAT4 FAT atypical cadherin 4
FOXG1 forkhead box G1
GPSM2 G-protein signaling modulator 2
L1CAM L1 cell adhesion molecule
MCOLN1 mucolipin 1
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NONO non-POU domain containing, octamer-binding
NT5C2 5'-nucleotidase, cytosolic II
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PYCR1 pyrroline-5-carboxylate reductase 1
SIN3A SIN3 transcription regulator family member A
SNAP29 synaptosomal-associated protein, 29kDa
SON SON DNA binding protein
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
TBCK TBC1 domain containing kinase
TUBA8 tubulin, alpha 8
ZNF462 zinc finger protein 462