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Immunogen sequence: ITYHAHLQGH PDLPRWLRYT QRSPHHPGFL YGSATPEDRG LQVIEVTAYN RDSFDTTRQR LVLEIGDPEG PLLPYQAEFL VRSHDAEEVL PSTPASRFLS ALGGLWEPGE LQLLNVTSAL DRGGRVPLPI EGRKEGVYIK VGSASPFSTC LKMVASPDSH ARCAQGQPPL LSCYDTLAPH FRVDWCNVTL VDKSVPEPAD EVPTPGDGIL EHDPFFCPPT EAPDRDFLVD A; Positive Samples: A-549, LO2, 293T, Mouse skeletal muscle, Mouse heart, Rat skeletal muscle, Rat heart; Cellular Location: Cell membrane, Cytoplasm, Single-pass type I membrane protein, cytoskeleton, sarcolemma
The sarcoglycan transmembrane proteins are members of the dystrophin complex. Sarcoglycans cluster together to form a complex, which is localized in the cell membrane of skeletal, cardiac, and smooth muscle fibers. Four sarcoglycan subunit proteins, designated alpha-, beta-, gamma- and delta-sarcoglycan, form a complex on the skeletal muscle cell surface membrane. A genetic defect in any one of these proteins causes the loss or marked decrease of the whole sarcoglycan complex, which is observed in the autosomal recessive muscular dystrophy, sarcoglycanopathy. In smooth muscle, beta- and delta-sarcoglycans are associated with epsilon-sarcoglycan, a glycoprotein homologous to alpha-sarcoglycan. Additionally, a complete deficiency in delta-sarcoglycan is the cause of the Syrian hamster BIO.14 cardiomyopathy.
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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: 50 kDa dystrophin-associated glycoprotein; 50DAG; 50kD DAG; Adhalin; Alpha-sarcoglycan; Alpha-SG; Dystroglycan 2; Dystroglycan-2; Dystroglycan2; limb girdle muscular dystrophy 2D; sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein); SG alpha; SG-alpha
基因别名: 50DAG; adhalin; ADL; Asg; DAG2; DMDA2; LGMD2D; SCARMD1; SGCA
UniProt ID: (Human) Q16586, (Mouse) P82350
Entrez Gene ID: (Human) 6442, (Rat) 303468, (Mouse) 20391