cd36l2 antikoerper, fi13c07 antikoerper, chunp6914 antikoerper, wu:fi13c07 antikoerper, SCARB2 antikoerper, scarb2 antikoerper, AMRF antikoerper, CD36L2 antikoerper, EPM4 antikoerper, HLGP85 antikoerper, LGP85 antikoerper, LIMP-2 antikoerper, LIMPII antikoerper, SR-BII antikoerper, 9330185J12Rik antikoerper, Cd36l2 antikoerper, MLGP85 antikoerper, LimpII antikoerper, scavenger receptor class B, member 2a antikoerper, scavenger receptor class B member 2 antikoerper, scavenger receptor class B, member 2 antikoerper, scarb2a antikoerper, SCARB2 antikoerper, scarb2 antikoerper, Scarb2 antikoerper
Hintergrund
The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alias Symbols: AMRF, CD36L2, EPM4, HLGP85, LGP85, LIMP-2, LIMPII, SR-BII Protein Interaction Partner: UBC, ATP4A, TAF15, NONO, HSPD1, DDX1, ATP6V1B1, Ap1g1, AP3S2, AP3S1, THBS1, Protein Size: 478