Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP.
A synthesized peptide derived from human NXNL2.
A synthesized peptide derived from human NXPH1, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human NXPH2, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human NXPH3, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human NXPH4, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human NXT2.
A synthesized peptide derived from human NYREN18, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human OAS1, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human OAS2, corresponding to a region within C-terminal amino acids.
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