Aliases for LIN7C Gene
External Ids for LIN7C Gene
Previous GeneCards Identifiers for LIN7C Gene
GeneCards Summary for LIN7C Gene
LIN7C (Lin-7 Homolog C (C. Elegans)) is a Protein Coding gene. Diseases associated with LIN7C include wagr syndrome and mood disorder. GO annotations related to this gene include protein domain specific binding and cytoskeletal protein binding. An important paralog of this gene is LIN7A.
UniProtKB/Swiss-Prot for LIN7C Gene
Plays a role in establishing and maintaining the asymmetric distribution of channels and receptors at the plasma membrane of polarized cells. Forms membrane-associated multiprotein complexes that may regulate delivery and recycling of proteins to the correct membrane domains. The tripartite complex composed of LIN7 (LIN7A, LIN7B or LIN7C), CASK and APBA1 may have the potential to couple synaptic vesicle exocytosis to cell adhesion in brain. Ensures the proper localization of GRIN2B (subunit 2B of the NMDA receptor) to neuronal postsynaptic density and may function in localizing synaptic vesicles at synapses where it is recruited by beta-catenin and cadherin. Required to localize Kir2 channels, GABA transporter (SLC6A12) and EGFR/ERBB1, ERBB2, ERBB3 and ERBB4 to the basolateral membrane of epithelial cells