absent third pharyngeal arch Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the structure of the third are which contributes to the development of the hyoid bone, stylopharyngeus muscle, inferior parathyroid gland, and thymus (Mammalian Phenotype Ontology, MP_0010642)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010642
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Genes

6 gene mutations causing the absent third pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
MED12 mediator complex subunit 12
PRDM1 PR domain containing 1, with ZNF domain
RDH10 retinol dehydrogenase 10 (all-trans)
TBX1 T-box 1