abnormal common lymphocyte progenitor cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a progenitor cell committed to the lymphoid lineage (Mammalian Phenotype Ontology, MP_0008249)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008249
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12 gene mutations causing the abnormal common lymphocyte progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID3A AT rich interactive domain 3A (BRIGHT-like)
BCL11A B-cell CLL/lymphoma 11A (zinc finger protein)
CXCL12 chemokine (C-X-C motif) ligand 12
FANCC Fanconi anemia, complementation group C
FLT3LG fms-related tyrosine kinase 3 ligand
HMGB3 high mobility group box 3
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
KIAA0101 KIAA0101
MSI2 musashi RNA-binding protein 2
MYB v-myb avian myeloblastosis viral oncogene homolog
SOD1 superoxide dismutase 1, soluble