abnormal alveolocapillary membrane morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the membrane between the capillary blood and alveolar air, comprised of the alveolar epithelium and the capillary epithelium and their adherent basement membranes and epithelial cell cytoplasm (Mammalian Phenotype Ontology, MP_0002324)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002324
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2 gene mutations causing the abnormal alveolocapillary membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CUX1 cut-like homeobox 1
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)