pharyngeal arch hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size of the transient structures of the embryo that develop into regions of the head, neck and ears, usually due to reduced cell number (Mammalian Phenotype Ontology, MP_0003873)
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11 gene mutations causing the pharyngeal arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
FOXO1 forkhead box O1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
HAND2 heart and neural crest derivatives expressed 2
HFM Hemifacial microsomia
KIF3A kinesin family member 3A
MECOM MDS1 and EVI1 complex locus
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
TDG thymine-DNA glycosylase
VEGFA vascular endothelial growth factor A