abnormal frontonasal prominence morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of an unpaired facial process in the embryo formed from the tissues surrounding the forebrain vesicle that develops into the forehead and bridge of the nose/snout (Mammalian Phenotype Ontology, MP_0009901)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009901
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Genes

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

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
APAF1 apoptotic peptidase activating factor 1
DKK1 dickkopf WNT signaling pathway inhibitor 1
DLX5 distal-less homeobox 5
HESX1 HESX homeobox 1
HHAT hedgehog acyltransferase
OPA1 optic atrophy 1 (autosomal dominant)
RDH10 retinol dehydrogenase 10 (all-trans)
TBC1D32 TBC1 domain family, member 32
TCOF1 Treacher Collins-Franceschetti syndrome 1