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Symbol Name ID |
Txn2
thioredoxin 2 MGI:1929468 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Increased CSF lactate |
Increased CSF protein concentration |
Spasticity |
Delayed CNS myelination |
Axonal degeneration |
Subependymal cysts |
Cerebellar atrophy |
Global brain atrophy |
Dystonia |
Global developmental delay |
Severe global developmental delay |
Peripheral neuropathy |
Seizure |
| Disease(s) Associated with TXN2 | ||||||||||||||
| combined oxidative phosphorylation deficiency 29 |
| Mouse Phenotypes | incomplete rostral neuropore closure |
exencephaly |
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| Availability | Mouse Genotype | ||
| Txn2Gt(OST69169)Lex/Txn2Gt(OST69169)Lex | |||
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 05/07/2024 MGI 6.23 |
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