Spinal Cord Myelodysplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0344479
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Genes

28 genes associated with the disease Spinal Cord Myelodysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BHMT betaine--homocysteine S-methyltransferase
CCL2 chemokine (C-C motif) ligand 2
CECR2 cat eye syndrome chromosome region, candidate 2
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
FOLR1 folate receptor 1 (adult)
FOLR2 folate receptor 2 (fetal)
FUZ fuzzy planar cell polarity protein
GHRL ghrelin/obestatin prepropeptide
GLI3 GLI family zinc finger 3
GRHL3 grainyhead-like 3 (Drosophila)
IFNG interferon, gamma
INS insulin
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
NPY1R neuropeptide Y receptor Y1
PAX3 paired box 3
PRSS8 protease, serine, 8
PYY peptide YY
RRM1 ribonucleotide reductase M1
SKI SKI proto-oncogene
SPINT2 serine peptidase inhibitor, Kunitz type, 2
T T, brachyury homolog (mouse)
VANGL1 VANGL planar cell polarity protein 1
VANGL2 VANGL planar cell polarity protein 2
ZIC2 Zic family member 2
ZIC5 Zic family member 5