| Human Disease |
Tietz Syndrome OMIM ID: 103500 |
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| Synonyms | Albinism-Deafness of Tietz; Hypopigmentation/Deafness of Tietz; Tietz Albinism-Deafness Syndrome | |||||||||||||||||||||
| View all models | View ALL (14) 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 |
| Mitfmi-x/Mitfmi-x |
NZB/Mac | J:83501 | View |
| MitfRorp/MitfRorp |
involves: BALB/cAnN * C3H/HeN | J:75964 | View |
| MitfMi-Crc/MitfMi-Crc |
CBA/CaCrc | J:83500 | View |
| MitfMi-H/MitfMi-H |
involves: BALB/cAnN * C3H/HeN | J:75964 | View |
| Mitfmi-enu122/Mitfmi-enu122 |
involves: 102 * C3H | J:46254 | View |
| MitfMi-Crc/Mitf+ |
CBA/CaCrc | J:83500 | View |
| MitfMi-H/Mitf+ |
involves: BALB/cAnN * C3H/HeN | J:75964 | View |
| Mitfmi-enu122/Mitf+ |
involves: 102 * C3H | J:46254 | View |
| MitfMi-wh/MitfMi-wh |
involves: C57BL * DBA | J:13058 | View |
| MitfMi-wh/Mitf+ |
involves: C57BL * DBA | J:13058 | View |
| MitfMi/MitfMi |
Not Specified | J:30758 | View |
| MitfRorp/Mitf+ |
involves: BALB/cAnN * C3H/HeN | J:75964 | View |
| MitfMi-wh/Mitfmi-x |
NZB/Mac | J:83501 | View |
| MitfMi-H/MitfRorp |
involves: BALB/cAnN * C3H/HeN | J:75964 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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