abnormal spleen mesenchyme morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the embryonic connective tissue made up of loosely aggregated mesenchymal cells, supported by interlaminar jelly, that gives rise to the developing spleen (Mammalian Phenotype Ontology, MP_0011263)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011263
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Genes

1 gene mutations causing the abnormal spleen mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
TLX1 T-cell leukemia homeobox 1