abnormal embryonic erythrocyte morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the embryonic blood cells that carry oxygen; embryonic erythrocytes arise from yolk sac blood islands and express different types of hemoglobins (beta-H1, gamma-1 and zeta) than adult erythrocytes, and can enucleate in circulation (Mammalian Phenotype Ontology, MP_0004230)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004230
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Genes

9 gene mutations causing the abnormal embryonic erythrocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EBP emopamil binding protein (sterol isomerase)
EPOR erythropoietin receptor
F3 coagulation factor III (thromboplastin, tissue factor)
FLT1 fms-related tyrosine kinase 1
FOSL1 FOS-like antigen 1
GFI1B growth factor independent 1B transcription repressor
KLF1 Kruppel-like factor 1 (erythroid)
TFRC transferrin receptor
TMOD1 tropomodulin 1