premaxilla hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, in the anterior and interior portion of the maxilla (Mammalian Phenotype Ontology, MP_0004871)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004871
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Genes

5 gene mutations causing the premaxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
DLG1 discs, large homolog 1 (Drosophila)
SATB2 SATB homeobox 2
TCOF1 Treacher Collins-Franceschetti syndrome 1
ZIC3 Zic family member 3