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Invitrogen
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Peptide sequence: GQMREAERQQ RERSNAVRKV CTGVDYSWLA STPRSTYDLS PIERLQLEDV
Sequence homology: Dog: 79%; Human: 100%
RD3 is preferentially expressed in retina.Defects in RD3 are the cause of Leber congenital amaurosis type 12 (LCA12).
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Protein RD3; Retinal degeneration protein 3
基因别名: C1orf36; LCA12; RD3
UniProt ID: (Human) Q7Z3Z2
Entrez Gene ID: (Human) 343035