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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Amelx
amelogenin, X-linked
MGI:88005
13 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Amelxtm1Kul/Amelxtm1Kul
Tg(AMELX*P70T)2Gibs/?
involves: 129S1/Sv * 129X1/SvJ
abnormal enamel morphology J:122914
increased tumor incidence J:122914
Amelxtm1Kul/Amelxtm1Kul
Tg(AMELX-LRAP)9Gibs/0
involves: 129S1/Sv * 129X1/SvJ
abnormal enamel morphology J:122916
abnormal enamel rod pattern J:122916
reduced enamel thickness J:122916
Amelxtm1Msnd/Amelx+
involves: 129X1/SvJ
abnormal enamel rod pattern J:116448
brittle teeth J:116448
Amelxtm1Msnd/Amelxtm1Msnd
involves: 129X1/SvJ
abnormal ameloblast morphology J:116448
abnormal enamel morphology J:116448
abnormal enamel rod pattern J:116448
abnormal molar cusp morphology J:116448
abnormal tooth wear J:116448
brittle teeth J:116448
reduced enamel thickness J:116448
short Tomes' process J:116448
Amelxtm2Msnd/Amelx+
involves: 129X1/SvJ
abnormal enamel rod pattern J:116448
brittle teeth J:116448
Amelxtm2Msnd/Amelxtm2Msnd
involves: 129X1/SvJ
abnormal ameloblast morphology J:116448
abnormal enamel morphology J:116448
abnormal enamel rod pattern J:116448
abnormal molar crown morphology J:116448
abnormal tooth wear J:116448
brittle teeth J:116448
reduced enamel thickness J:116448
short Tomes' process J:116448
Amelxtm3Msnd/Amelxtm3Msnd
involves: 129X1/SvJ * C57BL/6
reduced enamel thickness J:170226
Tg(AMELX*M180)87Gibs/?
Not Specified
normal craniofacial phenotype J:122914
Tg(AMELX*P70T)2Gibs/?
Not Specified
abnormal enamel rod pattern J:122914
abnormal molar cusp morphology J:122914
abnormal molar morphology J:122914
abnormal tooth attrition J:122914

Contributing Projects:
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
11/19/2024
MGI 6.24
The Jackson Laboratory