半岛bd体育手机客户端
介绍 基因名： Atp6v0a2 半岛bd体育手机客户端 别名： 8430408C20Rik； AI385560； ATP6a2； AW489264； Atp6n1d； Atp6n2； C76904； ISF； J6B7； SHIF； Stv1； TJ6M； TJ6s； Tj6； V-ATPase 116 kDa； V-ATPase a2； Atp6v0a2； ATPase, H+ transporting, lysosomal V0 subunit A2； ATPase, H+ transporting, lysosomal V0 subunit A2； V-type proton ATPase 116 kDa subunit a 2； ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 2 (38kD)； ATPase, H+ transporting, lysosomal V0 subunit a； T-cell expressing clone j6； V-ATPase 116 kDa subunit a 2； V-ATPase 116 kDa subunit a2； V-type proton ATPase 116 kDa subunit a； V-type proton ATPase 116 kDa subunit a2； immune suppressor factor J6B7； lysosomal H(+)-transporting ATPase V0 subunit a 2； vacuolar proton translocating ATPase 116 kDa subunit a； 液泡膜质子转运ATP酶2型； 背景信息： The protein encoded by this gene is a subunit of the vacuolar ATPase (v-ATPase), an heteromultimeric enzyme that is present in intracellular vesicles and in the plasma membrane of specialized cells, and which is essential for the acidification of diverse cellular components. V-ATPase is comprised of a membrane peripheral V(1) domain for ATP hydrolysis, and an integral membrane V(0) domain for proton translocation. The subunit encoded by this gene is a component of the V(0) domain. Mutations in this gene are a cause of both cutis laxa type II and wrinkly skin syndrome. [provided by RefSeq, Jul 2009] 标签：His-tag |
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