Atrophy 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/C0431370
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Genes

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

Symbol Name
AIMP1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ANPEP alanyl (membrane) aminopeptidase
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
BCAP31 B-cell receptor-associated protein 31
CACNA1E calcium channel, voltage-dependent, R type, alpha 1E subunit
CNTNAP1 contactin associated protein 1
DNM1L dynamin 1-like
EMC1 ER membrane protein complex subunit 1
FA2H fatty acid 2-hydroxylase
GBA2 glucosidase, beta (bile acid) 2
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
IRF2BPL interferon regulatory factor 2 binding protein-like
KIF1A kinesin family member 1A
L2HGDH L-2-hydroxyglutarate dehydrogenase
LMNB1 lamin B1
MAG myelin associated glycoprotein
OPA1 optic atrophy 1 (autosomal dominant)
PEX16 peroxisomal biogenesis factor 16
SPG11 spastic paraplegia 11 (autosomal recessive)
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase