abnormal maxillary prominence morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the paired dorsal prominences formed by bifurcation of the first pharyngeal arches in the embryo that unite with the ipsilateral medial nasal process to form the upper jaw (Mammalian Phenotype Ontology, MP_0010940)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010940
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Genes

8 gene mutations causing the abnormal maxillary prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
HHAT hedgehog acyltransferase
MTHFD1L methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like
OTX2 orthodenticle homeobox 2
RDH10 retinol dehydrogenase 10 (all-trans)
RSPO2 R-spondin 2
TCOF1 Treacher Collins-Franceschetti syndrome 1