abnormal fetal liver hematopoietic progenitor cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a hematopoietic stem cell that resides in the fetal liver (Mammalian Phenotype Ontology, MP_0011246)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011246
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Genes

3 gene mutations causing the abnormal fetal liver hematopoietic progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BRD1 bromodomain containing 1
MECOM MDS1 and EVI1 complex locus
SCMH1 sex comb on midleg homolog 1 (Drosophila)