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Proteintech
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Immunogen sequence: MLVTLGLLT SFFSFLYMVA PSIRKFFAGG VCRTNVQLPG KVVVITGANT GIGKETAREL ASRGARVYIA CRDVLKGESA ASEIRVDTKN SQVLVRKLDL SDTKSIRAFA EGFLAEEKQL HILINNAGVM MCPYSKTADG FETHLGVNHL GHFLLTYLLL EQLKVSAPAR VVNVSSVAHH IGKIPFHDLQ SEKRYSRGFA YCHSKLANVL FTRELAKRLQ GTGVTTYAVH PGVVRSELVR HSSLLCLLWR LFSPFVKTAR EGAQTSLHCA LAEGLEPLSG KYFSDCKRTW VSPRARNNKT AERLWNVSCE LLGIRWE (1-316 aa encoded by BC025724)
The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).
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: All-trans and 9-cis retinol dehydrogenase; LCA3; Retinol dehydrogenase 12; retinol dehydrogenase 12, all-trans and 9-cis; Short chain dehydrogenase/reductase family 7C member 2; short chain dehydrogenase/reductase family 7C, member 2
基因别名: A930033N07Rik; LCA13; RDH12; RP53; SDR7C2
UniProt ID: (Human) Q96NR8, (Mouse) Q8BYK4
Entrez Gene ID: (Human) 145226, (Rat) 314264, (Mouse) 77974