abnormal cellular hemoglobin content Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the mean of the red blood cell hemoglobin concentration (RBC CH) histogram, which represents the distribution of red blood cells by the amount of hemoglobin present in each individual cell independent of cell volume (Mammalian Phenotype Ontology, MP_0008954)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008954
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Genes

11 gene mutations causing the abnormal cellular hemoglobin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANK1 ankyrin 1, erythrocytic
EPB41 erythrocyte membrane protein band 4.1
JAK1 Janus kinase 1
KEL Kell blood group, metallo-endopeptidase
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
SLC25A37 solute carrier family 25 (mitochondrial iron transporter), member 37
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
TFR2 transferrin receptor 2
TMEM14C transmembrane protein 14C