| Human Disease |
Laron Syndrome OMIM ID: 262500 |
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| Synonyms | Growth Hormone Insensitivity Syndrome; Growth Hormone Receptor Deficiency; Pituitary Dwarfism II | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Ghrtm1Arge/Ghrtm1Arge |
involves: 129S/SvEv * C57BL/6J | J:66913 | View |
| Ghrtm1Jjk/Ghrtm1Jjk |
involves: 129P2/OlaHsd * BALB/c | J:44604, J:157146 | 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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