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Symbol Name ID |
Fam20c
FAM20C, golgi associated secretory pathway kinase MGI:2136853 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal jaw morphology |
Taurodontia |
Abnormal permanent molar morphology |
Fragile teeth |
Multiple unerupted teeth |
Enamel hypomineralization |
Hypocalcification of dental enamel |
Hypomature dental enamel |
Enamel hypoplasia |
Abnormal dentin morphology |
Abnormality of dental color |
Yellow-brown discoloration of the teeth |
Hypoplasia of teeth |
Anterior open-bite malocclusion |
Widely spaced teeth |
Impaired mastication |
| Disease(s) Associated with FAM20C | ||||||||||||||||
| amelogenesis imperfecta |
| Mouse Phenotypes | dental pulp necrosis |
periodontal ligament necrosis |
small cranium |
abnormal jaw morphology |
alveolar process atrophy |
abnormal tooth morphology |
abnormal dental pulp cavity morphology |
conical molar |
small molars |
abnormal periodontal ligament morphology |
abnormal dentin development |
abnormal tooth hard tissue morphology |
abnormal cementum morphology |
abnormal dentin morphology |
absent enamel |
abnormal tooth root morphology |
tooth abscess |
apical tooth abscess |
mandibular hyperostosis |
abnormal maxilla morphology |
flat face |
detached junctional epithelium |
periodontal pocket |
short snout |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||
| Fam20ctm1Lex/Fam20ctm1Lex | |||||||||||||||||||||||||
| Fam20ctm1.1Cqi/Fam20ctm1.1Cqi Edil3Tg(Sox2-cre)1Amc/Edil3+ (conditional) |
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| Fam20ctm1.1Cqi/Fam20ctm1.1Cqi Tg(Col1a1-cre)2Bek/0 (conditional) |
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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