microcytic anemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11252)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001935
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25 genes associated with the microcytic 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
ACVRL1 activin A receptor type II-like 1
AGGF1 angiogenic factor with G patch and FHA domains 1
ALAS2 5'-aminolevulinate synthase 2
ATRX alpha thalassemia/mental retardation syndrome X-linked
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
ENG endoglin
FECH ferrochelatase
GDF2 growth differentiation factor 2
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
HBB hemoglobin, beta
HBD hemoglobin, delta
HBG1 hemoglobin, gamma A
IRX5 iroquois homeobox 5
LCRB locus control region, beta
LPIN2 lipin 2
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
PUS1 pseudouridylate synthase 1
SMAD4 SMAD family member 4
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal
SRD5A3 steroid 5 alpha-reductase 3
TMPRSS6 transmembrane protease, serine 6
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1