Delayed Cns Myelination Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Delayed myelination in the central nervous system. (Human Phenotype Ontology, HP_0002188)
External Link https://www.disgenet.org/browser/0/1/0/C4021758
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Genes

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

Symbol Name
ACY1 aminoacylase 1
ALG9 ALG9, alpha-1,2-mannosyltransferase
BMP4 bone morphogenetic protein 4
CNTNAP1 contactin associated protein 1
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
D2HGDH D-2-hydroxyglutarate dehydrogenase
FOXG1 forkhead box G1
ITPA inosine triphosphatase (nucleoside triphosphate pyrophosphatase)
KDM1A lysine (K)-specific demethylase 1A
MMUT methylmalonyl-CoA mutase
PEX7 peroxisomal biogenesis factor 7
POGZ pogo transposable element with ZNF domain
SLC12A5 solute carrier family 12 (potassium/chloride transporter), member 5
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SMG9 SMG9 nonsense mediated mRNA decay factor
TBC1D24 TBC1 domain family, member 24
TXN2 thioredoxin 2
UBA5 ubiquitin-like modifier activating enzyme 5
UPB1 ureidopropionase, beta
VPS11 vacuolar protein sorting 11 homolog (S. cerevisiae)