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Symbol Name ID |
Slc33a1
solute carrier family 33 (acetyl-CoA transporter), member 1 MGI:1332247 |
| Darker colors indicate more annotations |
| Human Phenotypes | Lower limb spasticity |
Spastic paraplegia |
Progressive spastic paraplegia |
Spastic gait |
Degeneration of the lateral corticospinal tracts |
Spinal cord lesion |
Clonus |
Babinski sign |
Hyperreflexia |
Lower limb hyperreflexia |
Impaired vibration sensation in the lower limbs |
| Disease(s) Associated with SLC33A1 | |||||||||||
| hereditary spastic paraplegia 42 |
| Mouse Phenotypes | microgliosis |
brain inflammation |
abnormal corpus callosum morphology |
decreased corpus callosum size |
astrocytosis |
gliosis |
neuron degeneration |
abnormal spinal cord white matter morphology |
spinal cord degeneration |
neurodegeneration |
axon degeneration |
demyelination |
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| Availability | Mouse Genotype | ||||||||||||
| Slc33a1tm1.1Lpu/Slc33a1+ | |||||||||||||
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 05/14/2024 MGI 6.23 |
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