Megaloblastic Anemia Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production. (Human Disease Ontology, DOID_13382)
External Link	https://www.disgenet.org/browser/0/1/0/C0543641
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Genes

12 genes associated with the disease Megaloblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
AMN	amnion associated transmembrane protein
CUBN	cubilin (intrinsic factor-cobalamin receptor)
DHFR	dihydrofolate reductase
GIF	gastric intrinsic factor (vitamin B synthesis)
HP	haptoglobin
IGF1	insulin-like growth factor 1 (somatomedin C)
MIF	macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MT3	metallothionein 3
MTHFD1	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTR	5-methyltetrahydrofolate-homocysteine methyltransferase
NDUFB3	NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa
TNFAIP1	tumor necrosis factor, alpha-induced protein 1 (endothelial)