RARS2 Back

arginyl-tRNA synthetase 2, mitochondrial

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NCBI Description of RARS2
The protein encoded by this gene is an arginyl-tRNA synthetase that is found in the mitochondrial matrix. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6).

Community Annotation of RARS2 Add / Edit RARS2: Annotations

No community annotations yet for RARS2.
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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

RARS2 is highly significantly mutated in
(none)
RARS2 is significantly mutated in
(none)
RARS2 is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for RARS2