hypochromic anemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001931
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16 genes associated with the hypochromic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7
ALAS2 5'-aminolevulinate synthase 2
ATRX alpha thalassemia/mental retardation syndrome X-linked
CASP10 caspase 10, apoptosis-related cysteine peptidase
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
IRX5 iroquois homeobox 5
LCRB locus control region, beta
PUS1 pseudouridylate synthase 1
STK11 serine/threonine kinase 11
TF transferrin
TMPRSS6 transmembrane protease, serine 6
WAS Wiskott-Aldrich syndrome