increased mean corpuscular hemoglobin concentration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the normal Hgb/Hct; the average hemoglobin concentration in a given volume of packed red cells, calculated from the hemoglobin therein and the hematocrit, in erythrocyte indices (Mammalian Phenotype Ontology, MP_0005641)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005641
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Genes

25 gene mutations causing the increased mean corpuscular hemoglobin concentration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADD1 adducin 1 (alpha)
ADD2 adducin 2 (beta)
ATP8A1 ATPase, aminophospholipid transporter (APLT), class I, type 8A, member 1
B9D1 B9 protein domain 1
C1QBP complement component 1, q subcomponent binding protein
CDK6 cyclin-dependent kinase 6
CLK1 CDC-like kinase 1
EPB42 erythrocyte membrane protein band 4.2
FAM63A family with sequence similarity 63, member A
GRHL3 grainyhead-like 3 (Drosophila)
IFT20 intraflagellar transport 20
KCNJ12 potassium channel, inwardly rectifying subfamily J, member 12
KDM8 lysine (K)-specific demethylase 8
KEL Kell blood group, metallo-endopeptidase
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
MYSM1 Myb-like, SWIRM and MPN domains 1
NR1D2 nuclear receptor subfamily 1, group D, member 2
SKIDA1 SKI/DACH domain containing 1
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
ULK1 unc-51 like autophagy activating kinase 1
USP3 ubiquitin specific peptidase 3
XBP1 X-box binding protein 1
YIPF1 Yip1 domain family, member 1
ZC3HC1 zinc finger, C3HC-type containing 1