abnormal epidermal lamellar body morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a membrane-bounded organelle present in the epidermis, specialized for the storage and secretion of various substances (such as glycoproteins and acid phosphates), and which are arranged in the form of tightly packed, concentric, membrane sheets or lamellae (Mammalian Phenotype Ontology, MP_0009608)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009608
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Genes

6 gene mutations causing the abnormal epidermal lamellar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
CD44 CD44 molecule (Indian blood group)
CERS3 ceramide synthase 3
DGAT2 diacylglycerol O-acyltransferase 2
ELOVL1 ELOVL fatty acid elongase 1
RARG retinoic acid receptor, gamma