microcytic anemia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11252)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002810
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19 gene mutations causing the microcytic 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
CP ceruloplasmin (ferroxidase)
EXOC6 exocyst complex component 6
HMOX1 heme oxygenase 1
IL10 interleukin 10
JAK1 Janus kinase 1
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
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
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPTA1 spectrin, alpha, erythrocytic 1
STEAP3 STEAP family member 3, metalloreductase
TAL1 T-cell acute lymphocytic leukemia 1
TFRC transferrin receptor
TMPRSS6 transmembrane protease, serine 6
UROS uroporphyrinogen III synthase