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The protein encoded by ZNF513 is a possible transcriptional regulator involved in retinal development. Additionally we are shipping Zinc Finger Protein 513 Antibodies (8) and Zinc Finger Protein 513 Proteins (2) and many more products for this protein.
These results suggest that the ZNF513 p.C339R mutation is responsible for retinitis pigmentosa and that ZNF513 plays a key role in the regulation of photoreceptor-specific genes in retinal development and photoreceptor maintenance.
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.
novel zinc finger protein