| Human Disease |
Focal Facial Dermal Dysplasia 3, Setleis Type; FFDD3 OMIM ID: 227260 |
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| Synonyms | Bitemporal Forceps Marks Syndrome; Facial Ectodermal Dysplasia; Focal Facial Dermal Dysplasia, Type II, Formerly; Setleis Syndrome | |||||||||||||||||||||
| View all models | View ALL (1) 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 |
| Twist2tm1(cre)Dor/Twist2tm1(cre)Dor |
involves: 129X1/SvJ * C57BL/6 | J:169191 | 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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