palatal shelf hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the palatal projections from the inner part of the maxillary processes that fuse to form the secondary palate, often due to reduced cell number (Mammalian Phenotype Ontology, MP_0009883)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009883
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Genes

10 gene mutations causing the palatal shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
HAND2 heart and neural crest derivatives expressed 2
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
MSX1 msh homeobox 1
PBX1 pre-B-cell leukemia homeobox 1
PDGFC platelet derived growth factor C
PTCH1 patched 1
SIM2 single-minded family bHLH transcription factor 2
TBX2 T-box 2
TMEM107 transmembrane protein 107