| Human Disease |
Tooth Agenesis, Selective, 1; STHAG1 OMIM ID: 106600 |
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| Synonyms | Hypodontia/Oligodontia 1; HYD1; Second Premolars and Third Molars, Absence of | |||||||||||||||||||||
| View all models | View ALL (3) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Msx1tm1Bero/Msx1tm1Bero |
B6.129P2-Msx1tm1Bero | J:42035 | View |
| Msx1tm1Rilm/Msx1tm1Rilm |
either: (involves: 129S4/SvJae-Msx1tm1Rilm) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J) | J:17489 | View |
| Msx1tm1Rilm/Msx1tm1Rilm Msx2tm1Rilm/Msx2tm1Rilm |
involves: BALB/c * CD-1 | J:61509 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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