increased mean corpuscular hemoglobin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the average levels of hemoglobin contained in an erythrocyte (Mammalian Phenotype Ontology, MP_0005561)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005561
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Genes

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

Symbol Name
BBS5 Bardet-Biedl syndrome 5
CDK5RAP2 CDK5 regulatory subunit associated protein 2
CHSY1 chondroitin sulfate synthase 1
DKK3 dickkopf WNT signaling pathway inhibitor 3
ELK4 ELK4, ETS-domain protein (SRF accessory protein 1)
ELMO1 engulfment and cell motility 1
ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1
EPB41 erythrocyte membrane protein band 4.1
FAM53B family with sequence similarity 53, member B
FAM63A family with sequence similarity 63, member A
FOXO3 forkhead box O3
GALC galactosylceramidase
IL2 interleukin 2
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KEL Kell blood group, metallo-endopeptidase
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
KLF13 Kruppel-like factor 13
LCN2 lipocalin 2
MGAT4B mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B
MYO1C myosin IC
MYSM1 Myb-like, SWIRM and MPN domains 1
NPTN neuroplastin
PRKG1 protein kinase, cGMP-dependent, type I
SKIDA1 SKI/DACH domain containing 1
STK16 serine/threonine kinase 16
USP3 ubiquitin specific peptidase 3