Symbol Name ID |
Rnf170
ring finger protein 170 MGI:1924983 |
Darker colors indicate more annotations |
Human Phenotypes | Torticollis |
Lower limb muscle weakness |
Lower limb spasticity |
Spastic paraplegia |
Upper limb spasticity |
Frequent falls |
Generalized amyotrophy |
Disease(s) Associated with RNF170 | |||||||
autosomal dominant sensory ataxia 1 | |||||||
hereditary spastic paraplegia 85 |
Mouse Phenotypes | abnormal muscle physiology |
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Availability | Mouse Genotype | |
Rnf170Gt(OST104375)Lex/Rnf170Gt(OST104375)Lex |
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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