absent palatal shelf Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the palatal projections from the inner part of the maxillary processes that fuse to form the secondary palate (Mammalian Phenotype Ontology, MP_0009882)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009882
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4 gene mutations causing the absent palatal shelf phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
DLX2 distal-less homeobox 2
EFNB1 ephrin-B1
PTCH1 patched 1