abnormal tooth root development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant or incomplete formation of the part of a tooth that is implanted in the gum; the root is normally located below the neck of the tooth, covered by cementum rather than enamel, and attached by the periodontal ligament to the alveolar bone (Mammalian Phenotype Ontology, MP_0011165)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011165
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4 gene mutations causing the abnormal tooth root development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CSF1 colony stimulating factor 1 (macrophage)
FAM20C family with sequence similarity 20, member C
NFIC nuclear factor I/C (CCAAT-binding transcription factor)
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3