| Human Disease |
Phenylketonuria; PKU OMIM ID: 261600 |
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| Synonyms | Oligophrenia Phenylpyruvica; PAH Deficiency; Phenylalanine Hydroxylase Deficiency | ||||||||||||||||||||||||||||||||
| View all models | View ALL (5) 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 |
| Pahenu3/Pahenu3 |
involves: BTBR | J:13320 | View |
| Pahenu2/Pahenu2 |
BTBR-Pahenu2/J | J:178269 | View |
| Pahenu2/Pahenu2 |
involves: BTBR | J:38411 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Pahenu1/Pahenu1 |
involves: 101 * C3H | J:38411 | View |
| Pahenu1/Pahenu2 |
involves: 101 * C3H * BTBR | J:62365 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Hnf1atm1Mya/Hnf1atm1Mya |
involves: 129S2/SvPas | J:31627 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| hph1/hph1 |
involves: C57BL/6 * CBA/Ca | J:9146, J:101792 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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