anemia due to reduced life span of red cells Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of anemia related to a reduction in the average life span of red blood cells in the peripheral circulation, which is normally around 120 days. (Human Phenotype Ontology, HP_0011895)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011895
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Genes

75 genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
ADA adenosine deaminase
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
ADAR adenosine deaminase, RNA-specific
AK1 adenylate kinase 1
ALAD aminolevulinate dehydratase
ALDOA aldolase A, fructose-bisphosphate
ANK1 ankyrin 1, erythrocytic
ATP7B ATPase, Cu++ transporting, beta polypeptide
BPGM 2,3-bisphosphoglycerate mutase
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD19 CD19 molecule
CD3G CD3g molecule, gamma (CD3-TCR complex)
CD40LG CD40 ligand
CD59 CD59 molecule, complement regulatory protein
CD81 CD81 molecule
COL4A1 collagen, type IV, alpha 1
CPOX coproporphyrinogen oxidase
CR2 complement component (3d/Epstein Barr virus) receptor 2
DGKE diacylglycerol kinase, epsilon 64kDa
EPB41 erythrocyte membrane protein band 4.1
EPB42 erythrocyte membrane protein band 4.2
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FECH ferrochelatase
FOXP3 forkhead box P3
G6PD glucose-6-phosphate dehydrogenase
GALT galactose-1-phosphate uridylyltransferase
GATA1 GATA binding protein 1 (globin transcription factor 1)
GCLC glutamate-cysteine ligase, catalytic subunit
GP1BA glycoprotein Ib (platelet), alpha polypeptide
GPI glucose-6-phosphate isomerase
GPX1 glutathione peroxidase 1
GSR glutathione reductase
GSS glutathione synthetase
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
HK1 hexokinase 1
HMOX1 heme oxygenase 1
ICOS inducible T-cell co-stimulator
IGHV4-34 immunoglobulin heavy variable 4-34
KMT2D lysine (K)-specific methyltransferase 2D
LCAT lecithin-cholesterol acyltransferase
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
MS4A1 membrane-spanning 4-domains, subfamily A, member 1
NBN nibrin
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
NT5C3A 5'-nucleotidase, cytosolic IIIA
PFKM phosphofructokinase, muscle
PGK1 phosphoglycerate kinase 1
PGM3 phosphoglucomutase 3
PIEZO1 piezo-type mechanosensitive ion channel component 1
PIGT phosphatidylinositol glycan anchor biosynthesis, class T
PKLR pyruvate kinase, liver and RBC
PNP purine nucleoside phosphorylase
PRKCD protein kinase C, delta
RAG1 recombination activating gene 1
RHAG Rh-associated glycoprotein
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
STIM1 stromal interaction molecule 1
STOM stomatin
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C
TNFSF12 tumor necrosis factor (ligand) superfamily, member 12
TPI1 triosephosphate isomerase 1
TREX1 three prime repair exonuclease 1
UROD uroporphyrinogen decarboxylase
UROS uroporphyrinogen III synthase
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1