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Symbol Name ID |
Fam20a
FAM20A, golgi associated secretory pathway pseudokinase MGI:2388266 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal dental enamel morphology |
Amelogenesis imperfecta |
| Disease(s) Associated with FAM20A | ||
| amelogenesis imperfecta type 1G |
| Mouse Phenotypes | abnormal tooth morphology |
abnormal incisor morphology |
abnormal lower incisor color |
abnormal upper incisor color |
abnormal molar morphology |
abnormal molar cusp morphology |
conical molar |
small molars |
abnormal ameloblast morphology |
abnormal enamel morphology |
abnormal enamel rod pattern |
absent enamel |
enamel pits |
abnormal tooth wear |
short tibia |
increased bone mineral content |
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| Availability | Mouse Genotype | ||||||||||||||||
| Fam20atm1b(KOMP)Wtsi/Fam20atm1b(KOMP)Wtsi | |||||||||||||||||
| Fam20atm1Lex/Fam20atm1Lex | |||||||||||||||||
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 04/23/2024 MGI 6.23 |
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