hemolytic anemia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A type of anemia caused by premature destruction of red blood cells (hemolysis). (Human Phenotype Ontology, HP_0001878)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001585
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32 gene mutations causing the hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ADD1 adducin 1 (alpha)
ANK1 ankyrin 1, erythrocytic
C3 complement component 3
CD47 CD47 molecule
CD59 CD59 molecule, complement regulatory protein
EPB41 erythrocyte membrane protein band 4.1
FCER1G Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide
FCGR1A Fc fragment of IgG, high affinity Ia, receptor (CD64)
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FOXO3 forkhead box O3
HBA1 hemoglobin, alpha 1
HK1 hexokinase 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
IL2 interleukin 2
IL2RA interleukin 2 receptor, alpha
IL2RB interleukin 2 receptor, beta
LAT linker for activation of T cells
LCAT lecithin-cholesterol acyltransferase
LDHA lactate dehydrogenase A
NFE2L2 nuclear factor, erythroid 2-like 2
PKLR pyruvate kinase, liver and RBC
PRDX1 peroxiredoxin 1
PRDX2 peroxiredoxin 2
PRKAA1 protein kinase, AMP-activated, alpha 1 catalytic subunit
PRKAG1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit
SLC20A1 solute carrier family 20 (phosphate transporter), member 1
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
UROS uroporphyrinogen III synthase