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Symbol Name ID |
Pdhx
pyruvate dehydrogenase complex, component X MGI:1351627 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Hypertelorism |
Abnormality of eye movement |
Esodeviation |
Nystagmus |
Pendular nystagmus |
Oculomotor apraxia |
Blindness |
Ptosis |
| Disease(s) Associated with PDHX | |||||||||
| pyruvate decarboxylase deficiency |
| Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
abnormal lens morphology |
cataract |
persistence of hyaloid vascular system |
abnormal retina morphology |
decreased total retina thickness |
abnormal vitreous body morphology |
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| Availability | Mouse Genotype | ||||||||
| Pdhxtm1b(EUCOMM)Hmgu/Pdhx+ | |||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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