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Symbol
Name
ID
Rnf170
ring finger protein 170
MGI:1924983
Phenotype annotations related to muscle
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
Availability Mouse Genotype
Rnf170Gt(OST104375)Lex/Rnf170Gt(OST104375)Lex

Contributing Projects:
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
The Jackson Laboratory