microcytic anemia Gene Set
Genes
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
|
