abnormal pulp cavity morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the central hollow space of a tooth (Mammalian Phenotype Ontology, MP_0002819)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002819
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6 gene mutations causing the abnormal pulp cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
CTSV cathepsin V
DMP1 dentin matrix acidic phosphoprotein 1
DSPP dentin sialophosphoprotein
FAM20C family with sequence similarity 20, member C
MAP3K11 mitogen-activated protein kinase kinase kinase 11