| Human Disease |
Pituitary Hormone Deficiency, Combined, 2; CPHD2 OMIM ID: 262600 |
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| Synonyms | Ateliotic Dwarfism with Hypogonadism; Hanhart Dwarfism; Panhypopituitarism; Pituitary Dwarfism III | ||||||||||||||||||||||||||||||||
| 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 |
| Hesx1tm1Icar/Hesx1tm1Icar |
involves: 129P2/OlaHsd * C57BL/6 | J:47920 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Smpd3tm1Wst/Smpd3tm1Wst |
involves: 129S1/Sv | J:97284 | 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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