| Human Disease |
Carney Complex, Type 1; CNC1 OMIM ID: 160980 |
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| Synonyms | Carney Myxoma-Endocrine Complex; Carney Syndrome; CAR; Lamb Syndrome; Myxoma, Spotty Pigmentation, and Endocrine Overactivity; Name Syndrome | |||||||||||||||||||||
| View all models | View ALL (4) 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 |
| Prkar1atm1.2Lsk/Prkar1atm1.2Lsk Tg(Tyr-cre)3Gfk/0 |
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:98799 | View |
| Prkar1atm1Gsm/Prkar1a+ |
involves: 129X1/SvJ | J:93393 | View |
| Prkar1atm1.1Lsk/Prkar1a+ |
involves: 129S1/Sv * 129X1/SvJ | J:98799 | View |
| Prkar1atm1.1Lsk/Prkar1a+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:160299 | 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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