congenital hemolytic anemia Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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28 genes involed in the disease congenital hemolytic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
ADA adenosine deaminase
AK1 adenylate kinase 1
ALDOA aldolase A, fructose-bisphosphate
ANK1 ankyrin 1, erythrocytic
BPGM 2,3-bisphosphoglycerate mutase
CD59 CD59 molecule, complement regulatory protein
CDAN1 codanin 1
EPB41 erythrocyte membrane protein band 4.1
EPB42 erythrocyte membrane protein band 4.2
G6PD glucose-6-phosphate dehydrogenase
GCLC glutamate-cysteine ligase, catalytic subunit
GPI glucose-6-phosphate isomerase
GSS glutathione synthetase
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5
KLF1 Kruppel-like factor 1 (erythroid)
LPIN2 lipin 2
PGK1 phosphoglycerate kinase 1
PIEZO1 piezo-type mechanosensitive ion channel component 1
PKLR pyruvate kinase, liver and RBC
SEC23B Sec23 homolog B (S. cerevisiae)
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
TPI1 triosephosphate isomerase 1