ZNF513 Back

zinc finger protein 513

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NCBI Description of ZNF513

The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene.

Community Annotation of ZNF513 Add / Edit ZNF513: Annotations

No community annotations yet for ZNF513.
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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).


ZNF513 is highly significantly mutated in
ZNF513 is significantly mutated in
ZNF513 is near significance in

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

Data details

Mutation list for ZNF513