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Proteintech
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Sequence of this protein is as follows: MRAGQQLASM LRWTRAWRLP REGLGPHGPS FARVPVAPSS SSGGRGGAEP RPLPLSYRLL DGEAALPAVV FLHGLFGSKT NFNSIAKILA QQTGRRVLTV DARNHGDSPH SPDMSYEIMS QDLQDLLPQL GLVPCVVVGH SMGGKTAMLL ALQRPELVER LIAVDISPVE STGVSHFATY VAAMRAINIA DELPRSRARK LADEQLSSVI QDMAVRQHLL TNLVEVDGRF VWRVNLDALT QHLDKILAFP QRQESYLGPT LFLLGGNSQF VHPSHHPEIM RLFPRAQMQT VPNAGHWIHA DRPQDFIAAI RGFLV
ABHDB encodes a protein containing an alpha/beta hydrolase fold domain. This protein is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
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: Abhydrolase domain-containing protein 11; Alpha/beta hydrolase domain-containing protein 11; protein ABHD11; sn-1-specific diacylglycerol lipase ABHD11; WBSCR21 form D; WBSCR21 form E; Williams Beuren syndrome chromosome region 21; Williams-Beuren syndrome chromosomal region 21 protein
基因别名: ABHD11; PP1226; WBSCR21
UniProt ID: (Human) Q8NFV4
Entrez Gene ID: (Human) 83451