pulmonary hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size, usually due an increased number of cells of the respiratory organ in all or part of the organ (Mammalian Phenotype Ontology, MP_0004202)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004202
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Genes

5 gene mutations causing the pulmonary hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FSTL1 follistatin-like 1
HCK HCK proto-oncogene, Src family tyrosine kinase
IGF2R insulin-like growth factor 2 receptor
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PDGFRA platelet-derived growth factor receptor, alpha polypeptide