hypochromic anemia Gene Set
Genes
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
|
