megaloblastic anemia Gene Set
Genes
16 genes associated with the megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AMN
|
amnion associated transmembrane protein
|
|
CUBN
|
cubilin (intrinsic factor-cobalamin receptor)
|
|
DHFR
|
dihydrofolate reductase
|
|
FTCD
|
formimidoyltransferase cyclodeaminase
|
|
GIF
|
gastric intrinsic factor (vitamin B synthesis)
|
|
HPRT1
|
hypoxanthine phosphoribosyltransferase 1
|
|
LMBRD1
|
LMBR1 domain containing 1
|
|
MMACHC
|
methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
|
|
MMADHC
|
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
|
|
MTR
|
5-methyltetrahydrofolate-homocysteine methyltransferase
|
|
MTRR
|
5-methyltetrahydrofolate-homocysteine methyltransferase reductase
|
|
PHGDH
|
phosphoglycerate dehydrogenase
|
|
SLC19A2
|
solute carrier family 19 (thiamine transporter), member 2
|
|
SLC46A1
|
solute carrier family 46 (folate transporter), member 1
|
|
UMPS
|
uridine monophosphate synthetase
|
|
WFS1
|
Wolfram syndrome 1 (wolframin)
|
