abnormal alveolar process morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the thickened ridge of bone in the mandible and maxilla that holds the tooth sockets (Mammalian Phenotype Ontology, MP_0004189)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004189
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17 gene mutations causing the abnormal alveolar process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CTSK cathepsin K
DMP1 dentin matrix acidic phosphoprotein 1
EDNRA endothelin receptor type A
IFNG interferon, gamma
IL10 interleukin 10
IL12B interleukin 12B
IL4 interleukin 4
INHBA inhibin, beta A
LEF1 lymphoid enhancer-binding factor 1
MSX1 msh homeobox 1
NFIC nuclear factor I/C (CCAAT-binding transcription factor)
PAX9 paired box 9
POSTN periostin, osteoblast specific factor
SH3BP2 SH3-domain binding protein 2
SLC39A13 solute carrier family 39 (zinc transporter), member 13
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
TNF tumor necrosis factor