abnormal transforming growth factor beta level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal concentration of a paracrine growth factor that has a potential role in embryonic development, cellular differentiation, hormone secretion, and immune function (Mammalian Phenotype Ontology, MP_0008836)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008836
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Genes

9 gene mutations causing the abnormal transforming growth factor beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ADAM17 ADAM metallopeptidase domain 17
CD44 CD44 molecule (Indian blood group)
DMD dystrophin
DTX1 deltex 1, E3 ubiquitin ligase
IL1R1 interleukin 1 receptor, type I
IL4R interleukin 4 receptor
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
SLPI secretory leukocyte peptidase inhibitor