7tng
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Kringle domain of human Receptor Tyrosine Kinase-Like Orphan Receptor 1 (ROR1)
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Structural highlights
DiseaseROR1_HUMAN The disease is caused by mutations affecting the gene represented in this entry. FunctionROR1_HUMAN Has very low kinase activity in vitro and is unlikely to function as a tyrosine kinase in vivo (PubMed:25029443). Receptor for ligand WNT5A which activate downstream NFkB signaling pathway and may result in the inhibition of WNT3A-mediated signaling (PubMed:25029443, PubMed:27162350). In inner ear, crucial for spiral ganglion neurons to innervate auditory hair cells (PubMed:27162350).[1] [2] References
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This page was last modified 17:05, 18 October 2023.