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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