hypochromic anemia Gene Set
Genes
17 gene mutations causing the hypochromic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ANK1
|
ankyrin 1, erythrocytic
|
|
ATP4A
|
ATPase, H+/K+ exchanging, alpha polypeptide
|
|
EXOC6
|
exocyst complex component 6
|
|
FECH
|
ferrochelatase
|
|
HEPH
|
hephaestin
|
|
IL10
|
interleukin 10
|
|
NCKAP1L
|
NCK-associated protein 1-like
|
|
PICALM
|
phosphatidylinositol binding clathrin assembly protein
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
SLC11A2
|
solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
|
|
SLC40A1
|
solute carrier family 40 (iron-regulated transporter), member 1
|
|
SPTA1
|
spectrin, alpha, erythrocytic 1
|
|
STEAP3
|
STEAP family member 3, metalloreductase
|
|
TF
|
transferrin
|
|
TFRC
|
transferrin receptor
|
|
TRAF6
|
TNF receptor-associated factor 6, E3 ubiquitin protein ligase
|
|
UROS
|
uroporphyrinogen III synthase
|
