abnormal erythroblast number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered number of the nucleated precursor of erythrocytes (Mammalian Phenotype Ontology, MP_0011177)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011177
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19 gene mutations causing the abnormal erythroblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANK1 ankyrin 1, erythrocytic
BNIP3L BCL2/adenovirus E1B 19kDa interacting protein 3-like
BRD1 bromodomain containing 1
CBFB core-binding factor, beta subunit
CD59 CD59 molecule, complement regulatory protein
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
DCC DCC netrin 1 receptor
DIAPH3 diaphanous-related formin 3
FBXO7 F-box protein 7
FGFRL1 fibroblast growth factor receptor-like 1
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KLF1 Kruppel-like factor 1 (erythroid)
LCN2 lipocalin 2
PDGFB platelet-derived growth factor beta polypeptide
PKLR pyruvate kinase, liver and RBC
SPTA1 spectrin, alpha, erythrocytic 1
TTC7A tetratricopeptide repeat domain 7A
UNC93B1 unc-93 homolog B1 (C. elegans)