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Symbol
Name
ID
Dmp1
dentin matrix protein 1
MGI:94910
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Craniosynostosis
Disease(s) Associated with DMP1
autosomal recessive hypophosphatemic rickets

Mouse Phenotypes
abnormal alveolar process morphology
alveolar process atrophy
abnormal dental pulp cavity morphology
decreased molar number
abnormal periodontal ligament morphology
abnormal cementoblast morphology
decreased cementoblast number
abnormal cementocyte dendritic process morphology
abnormal cementum mineralization
abnormal dentin development
abnormal dentin mineralization
abnormal predentin morphology
abnormal tooth mineralization
growth retardation of molars
abnormal acellular cementum morphology
abnormal cellular cementum morphology
abnormal cementocyte lacunocanalicular system morphology
abnormal cementocyte canaliculus morphology
abnormal cementocyte lacuna morphology
abnormal dentin morphology
reduced enamel thickness
misaligned teeth
abnormal periodontium morphology
Availability Mouse Genotype
Dmp1tm1Mis/Dmp1tm1Mis

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/13/2018
MGI 6.11
The Jackson Laboratory