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Details of SOD1 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| SOD1 | --- | P00441 | SODC_HUMAN | 6647
| Q16669
| Q16711 | Q6NR85 |
Phenotypes
Abnormality of central motor function, Abnormality of higher mental function, Abnormality of metabolism/homeostasis, Abnormality of movement, Abnormality of muscle physiology, Abnormality of pyramidal motor function, Abnormality of the abdomen, Abnormality of the abdominal organs, Abnormality of the central nervous system, Abnormality of the esophagus, Abnormality of the gastrointestinal tract, Abnormality of the larynx, Abnormality of the musculature, Abnormality of the nervous system, Abnormality of the respiratory system, Abnormality of the upper respiratory tract, Abnormality of the voice, All, Apnea, Autosomal dominant inheritance, Autosomal recessive inheritance, Behavioural/Psychiatric Abnormality, Dysarthria, Dysphagia, Dysphonia, Fasciculations, Functional respiratory abnormality, Hypertonia, Involuntary movements, Mode of inheritance, Muscle cramps, Neurological speech impairment, Phenotypic abnormality, Pseudobulbar paralysis, Pseudobulbar signs, Sleep apnea, Sleep disturbance, Spasticity.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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