abnormal spleen development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant formation or incomplete differentiation of the organ that filters blood and stores red corpuscles and platelets (Mammalian Phenotype Ontology, MP_0009323)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009323
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5 gene mutations causing the abnormal spleen development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TCF21 transcription factor 21
TLX1 T-cell leukemia homeobox 1
TWSG1 twisted gastrulation BMP signaling modulator 1
WT1 Wilms tumor 1