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Symbol Name ID |
Slc11a2
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 MGI:1345279 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hyposmia |
Dysphagia |
Spasticity |
Fatigable weakness of bulbar muscles |
Fatigable weakness of swallowing muscles |
Fatigable weakness of respiratory muscles |
Motor neuron atrophy |
Amyotrophic lateral sclerosis |
Neurodegeneration |
Bradykinesia |
Fasciculations |
Tremor |
Paralysis |
Babinski sign |
Dysarthria |
Language impairment |
Depression |
Emotional lability |
Anxiety |
Panic attack |
Hallucinations |
Atypical behavior |
Apathy |
Reduced social reciprocity |
Impulsivity |
Agitation |
Restless legs |
Cognitive impairment |
Dementia |
Frontal lobe dementia |
Frontotemporal dementia |
Short attention span |
Sleep abnormality |
Insomnia |
Hyperreflexia |
Jaw hyperreflexia |
Dyskinesia |
Dystonia |
Gait imbalance |
Postural instability |
Abnormal autonomic nervous system physiology |
| Disease(s) Associated with SLC11A2 | |||||||||||||||||||||||||||||||||||||||||
| amyotrophic lateral sclerosis | |||||||||||||||||||||||||||||||||||||||||
| Parkinson's disease |
| Mouse Phenotypes | decreased brain iron level |
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| Availability | Mouse Genotype | |
| Slc11a2tm2Nca/Slc11a2tm2Nca Tg(Vil1-cre)20Syr/? (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 04/23/2024 MGI 6.23 |
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