RecName: Full=Oxysterol-binding protein-related protein 2; Short=ORP-2 - Protein

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OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin. [Autophagy. 2022]
OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin.
Koh YI, Oh KS, Kim JA, Noh B, Choi HJ, Joo SY, Rim JH, Kim HY, Kim DY, Yu S, et al. Autophagy. 2022 Nov; 18(11):2593-2614. Epub 2022 Mar 6.
Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling. [JCI Insight. 2022]
Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling.
Shi H, Wang H, Zhang C, Lu Y, Yao J, Chen Z, Xing G, Wei Q, Cao X. JCI Insight. 2022 Feb 22; 7(4). Epub 2022 Feb 22.
The lipid transporter ORP2 regulates synaptic neurotransmitter release via two distinct mechanisms. [Cell Rep. 2022]
The lipid transporter ORP2 regulates synaptic neurotransmitter release via two distinct mechanisms.
Weber-Boyvat M, Kroll J, Trimbuch T, Olkkonen VM, Rosenmund C. Cell Rep. 2022 Dec 27; 41(13):111882.

RefSeq protein isoforms
See 3 reference sequence protein isoforms for the Osbpl2 gene.

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Mouse Genome Informatics (MGI) [Mouse Genome Informatics (MGI)]
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Protein