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Symbol Name ID |
Gclc
glutamate-cysteine ligase, catalytic subunit MGI:104990 |
| Darker colors indicate more annotations |
| Human Phenotypes | Spinocerebellar tract degeneration |
Late-onset spinocerebellar degeneration |
Ataxia |
Dysarthria |
Depression |
Anxiety |
Psychosis |
Intellectual disability |
Hyperreflexia |
Global developmental delay |
Dyslexia |
Peripheral neuropathy |
Polyneuropathy |
| Disease(s) Associated with GCLC | |||||||||||||
| cystic fibrosis | |||||||||||||
| glutamate-cysteine ligase deficiency |
| Mouse Phenotypes | abnormal cingulate gyrus morphology |
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| Availability | Mouse Genotype | |
| Gclctm1Tdal/Gclctm1Tdal Pvalbtm1(cre)Arbr/Pvalb+ (conditional) |
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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 05/21/2024 MGI 6.23 |
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