abnormal dentin morphology 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:0002818
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15 gene mutations causing the abnormal dentin morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
CSF1 colony stimulating factor 1 (macrophage)
DMP1 dentin matrix acidic phosphoprotein 1
DSPP dentin sialophosphoprotein
FAM20C family with sequence similarity 20, member C
ITGA11 integrin, alpha 11
NFIC nuclear factor I/C (CCAAT-binding transcription factor)
OSTM1 osteopetrosis associated transmembrane protein 1
PAX9 paired box 9
POSTN periostin, osteoblast specific factor
RUNX2 runt-related transcription factor 2
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SP3 Sp3 transcription factor
SP6 Sp6 transcription factor
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3