|
Symbol Name ID |
Abhd12
abhydrolase domain containing 12 MGI:1923442 |
| Darker colors indicate more annotations |
| Human Phenotypes | Spasticity |
Demyelinating peripheral neuropathy |
Cerebellar atrophy |
Ataxia |
Dysmetria |
Intention tremor |
Babinski sign |
Decreased nerve conduction velocity |
Dysarthria |
Hyperreflexia |
Hyporeflexia |
Sensorimotor neuropathy |
Distal sensory impairment |
| Disease(s) Associated with ABHD12 | |||||||||||||
| PHARC syndrome |
| Mouse Phenotypes | microgliosis |
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| Availability | Mouse Genotype | |
| Abhd12tm1Crv/Abhd12tm1Crv | ||
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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