absent pharyngeal arches Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing the transient structures of the embryo that develop into regions of the head, neck and ears (Mammalian Phenotype Ontology, MP_0003874)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003874
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Genes

10 gene mutations causing the absent pharyngeal arches phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
CHRD chordin
FOXI3 forkhead box I3
HAND2 heart and neural crest derivatives expressed 2
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
OTX2 orthodenticle homeobox 2
OVOL2 ovo-like zinc finger 2
PDPK1 3-phosphoinositide dependent protein kinase 1
RDH10 retinol dehydrogenase 10 (all-trans)
TBX1 T-box 1