RNF112 Back

ring finger protein 112

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NCBI Description of RNF112
This gene encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17.

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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

RNF112 is highly significantly mutated in
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RNF112 is significantly mutated in
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RNF112 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for RNF112