absent mandible Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the mandible. (Human Phenotype Ontology, HP_0009939)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000087
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Genes

15 gene mutations causing the absent mandible phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CHRD chordin
DKK1 dickkopf WNT signaling pathway inhibitor 1
FLVCR1 feline leukemia virus subgroup C cellular receptor 1
GJB2 gap junction protein, beta 2, 26kDa
GPC3 glypican 3
HAT1 histone acetyltransferase 1
HHAT hedgehog acyltransferase
LPAR4 lysophosphatidic acid receptor 4
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
OTX2 orthodenticle homeobox 2
PGAP1 post-GPI attachment to proteins 1
SMAD2 SMAD family member 2
TWSG1 twisted gastrulation BMP signaling modulator 1
ZIC5 Zic family member 5