重组膜相关磷脂转运蛋白
交货期：1周
产品别名：Recombinant PITPNM3
Recombinant PITPNM family member 3 protein
Recombinant PITPNM family member 3 protein
基因名：
产品别名：
背景信息：
PITPNM3
产品别名：
ACKR6； CORD5； NIR1； RDGBA3； PITPNM3； PITPNM family member 3； PITPNM family member 3； membrane-associated phosphatidylinositol transfer protein 3； NIR-1； PITPnm 3； PYK2 N-terminal domain-interacting receptor 1； atypical chemokine receptor 6； cone rod dystrophy 5； phosphatidylinositol transfer protein, membrane-associated 3； retinal degeneration B alpha 3； 膜相关磷脂转运蛋白；
背景信息：
Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro) (By similarity). Binds calcium ions.
Involvement in disease:
Defects in PITPNM3 are the cause of cone-rod dystrophy type 5 (CORD5) . CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration.
Involvement in disease:
Defects in PITPNM3 are the cause of cone-rod dystrophy type 5 (CORD5) . CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration.
产品发布日期：2026.06.22
广州伟伯科技有限公司