| Human Disease |
Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities OMIM ID: 262190 |
|||||||||||||||||||||
| Synonyms | Mendenhall Syndrome; Rabson-Mendenhall Syndrome | |||||||||||||||||||||
| View all models | View ALL (1) "NOT" mouse models for this human disease. No mouse models with similarity to the expected human disease phenotype are reported in MGI. | |||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Insrtm1Jja/Insrtm1Jja |
involves: 129S2/SvPas * C57BL/6 * DBA/2 | J:32538 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 05/08/2013 MGI 5.13 |
|
|
|
||