midline facial cleft Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A congenital malformation with a cleft (gap or opening) in the midline of the face. (Human Phenotype Ontology, HP_0100629)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000108
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13 gene mutations causing the midline facial cleft phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
APAF1 apoptotic peptidase activating factor 1
CECR2 cat eye syndrome chromosome region, candidate 2
FBXO11 F-box protein 11
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
RDH10 retinol dehydrogenase 10 (all-trans)
SHROOM3 shroom family member 3
SKI SKI proto-oncogene
TACC3 transforming, acidic coiled-coil containing protein 3
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
ZEB1 zinc finger E-box binding homeobox 1