absent keratohyalin granules Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the irregularly shaped basophilic granules in the cells of the stratum granulosum of the epidermis that may play a role in keratinization and barrier function (Mammalian Phenotype Ontology, MP_0009603)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009603
Similar Terms
Downloads & Tools

Genes

1 gene mutations causing the absent keratohyalin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1