abnormal basal lamina morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the sheet of extracellular matrix characteristically situated under epithelial cells, around muscles, nerves, capillaries, and fat cells, and situated between these elements and the underlying or surrounding connective tissue (Mammalian Phenotype Ontology, MP_0004273)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004273
Similar Terms
Downloads & Tools


4 gene mutations causing the abnormal basal lamina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
LAMA2 laminin, alpha 2
LAMC2 laminin, gamma 2
RECK reversion-inducing-cysteine-rich protein with kazal motifs