abnormal erythroblast morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the nucleated precursor of erythrocytes (Mammalian Phenotype Ontology, MP_0011176)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011176
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Genes

25 gene mutations causing the abnormal erythroblast morphology 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
IKZF1 IKAROS family zinc finger 1 (Ikaros)
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
SAMD9L sterile alpha motif domain containing 9-like
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPTA1 spectrin, alpha, erythrocytic 1
TDP2 tyrosyl-DNA phosphodiesterase 2
TMOD3 tropomodulin 3 (ubiquitous)
TRPC2 transient receptor potential cation channel, subfamily C, member 2, pseudogene
TTC7A tetratricopeptide repeat domain 7A
UNC93B1 unc-93 homolog B1 (C. elegans)