Abnormal Cns Myelination Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of myelination of nerves in the central nervous system. (Human Phenotype Ontology, HP_0011400)
External Link https://www.disgenet.org/browser/0/1/0/C4021152
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Genes

9 genes associated with the disease Abnormal Cns Myelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTL6B actin-like 6B
ERCC3 excision repair cross-complementation group 3
FOXG1 forkhead box G1
GAA glucosidase, alpha; acid
GPT2 glutamic pyruvate transaminase (alanine aminotransferase) 2
IDUA iduronidase, alpha-L-
KIDINS220 kinase D-interacting substrate, 220kDa
SHPK sedoheptulokinase
UNC80 unc-80 homolog (C. elegans)