hypochromic microcytic anemia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A microcytic anemia characterized by paler than normal blood cells. (Human Disease Ontology, DOID_0050642)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008388
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9 gene mutations causing the hypochromic microcytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide
NCKAP1L NCK-associated protein 1-like
PICALM phosphatidylinositol binding clathrin assembly protein
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
TFRC transferrin receptor
UROS uroporphyrinogen III synthase