absent incisors Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000125
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21 gene mutations causing the absent incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2A activin A receptor, type IIA
BMP7 bone morphogenetic protein 7
CDON cell adhesion associated, oncogene regulated
CSF1 colony stimulating factor 1 (macrophage)
DISP1 dispatched homolog 1 (Drosophila)
EDA ectodysplasin A
EDAR ectodysplasin A receptor
FST follistatin
FUZ fuzzy planar cell polarity protein
GLI2 GLI family zinc finger 2
INHBA inhibin, beta A
LEF1 lymphoid enhancer-binding factor 1
MSX1 msh homeobox 1
NFIC nuclear factor I/C (CCAAT-binding transcription factor)
OSTM1 osteopetrosis associated transmembrane protein 1
PAX9 paired box 9
PC pyruvate carboxylase
SATB2 SATB homeobox 2
SRC SRC proto-oncogene, non-receptor tyrosine kinase
TRAF6 TNF receptor-associated factor 6, E3 ubiquitin protein ligase
VEGFA vascular endothelial growth factor A