abnormal diaphragm development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description malformation or incomplete differentiation of the thin musculomembranous barrier separating the abdominal and thoracic cavities and functioning in respiration (Mammalian Phenotype Ontology, MP_0012251)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012251
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11 gene mutations causing the abnormal diaphragm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFRL1 fibroblast growth factor receptor-like 1
FREM1 FRAS1 related extracellular matrix 1
GAB1 GRB2-associated binding protein 1
KIF7 kinesin family member 7
LOX lysyl oxidase
MET MET proto-oncogene, receptor tyrosine kinase
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
PAX3 paired box 3
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
SLIT3 slit homolog 3 (Drosophila)
WT1 Wilms tumor 1