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The following pages link to COPII

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• Hemophagocytic lymphohistiocytosis (links | edit)
• Vesicular transport protein (links | edit)
• Lysosomal trafficking regulator (links | edit)
• STX11 (links | edit)
• Nucleoporin (links | edit)
• VPS13B (links | edit)
• Caveolin 1 (links | edit)
• STX1A (links | edit)
• COPB1 (links | edit)
• DNM2 (links | edit)
• RAB3A (links | edit)
• STX4 (links | edit)
• SYT1 (links | edit)
• Biogenesis of lysosome-related organelles complex 1 (links | edit)
• CLTC (links | edit)
• DNM1 (links | edit)
• VAMP2 (links | edit)
• LMAN1 (links | edit)
• USO1 (links | edit)
• Perilipin-3 (links | edit)
• STX7 (links | edit)
• STX6 (links | edit)
• COPE (gene) (links | edit)
• AP3B1 (links | edit)
• VAMP3 (links | edit)
• STX5 (links | edit)
• COPB2 (links | edit)
• STX2 (links | edit)
• COPG2 (links | edit)
• COPG (links | edit)
• STX12 (links | edit)
• STX8 (links | edit)
• Syntaxin binding protein 2 (links | edit)
• DNM3 (links | edit)
• AP1S2 (links | edit)
• SNAP29 (links | edit)
• SYT2 (links | edit)
• SEC31A (links | edit)
• SYT3 (links | edit)
• SEC23A (redirect page) (links | edit)
  • Charcot–Marie–Tooth disease (links | edit)
  • Congenital disorder of glycosylation (links | edit)
  • Caveolae (links | edit)
  • Hereditary spastic paraplegia (links | edit)
  • Long QT syndrome (links | edit)
  • Small GTPase (links | edit)
  • Limb–girdle muscular dystrophy (links | edit)
  • Clathrin (links | edit)
  • COPII (links | edit)
  • COPI (links | edit)
  • Synaptic vesicle (links | edit)
  • Rab (G-protein) (links | edit)
  • Receptor-mediated endocytosis (links | edit)
  • Caveolin (links | edit)
  • Spinocerebellar ataxia (links | edit)
  • SNARE protein (links | edit)
  • Vesicle-associated membrane protein (links | edit)
  • Synaptobrevin (links | edit)
  • Chédiak–Higashi syndrome (links | edit)
  • Retromer (links | edit)
  • Transporter Classification Database (links | edit)
  • Hermansky–Pudlak syndrome (links | edit)
  • Choroideremia (links | edit)
  • Cohen syndrome (links | edit)
  • Dynamin (links | edit)
  • Griscelli syndrome (links | edit)
  • ADP ribosylation factor (links | edit)
  • SNAP25 (links | edit)
  • Synaptotagmin (links | edit)
  • Caveolin 3 (links | edit)
  • Archain (links | edit)
  • Coatomer (links | edit)
  • Hemophagocytic lymphohistiocytosis (links | edit)
  • Vesicular transport protein (links | edit)
  • Lysosomal trafficking regulator (links | edit)
  • STX11 (links | edit)
  • VPS13B (links | edit)
  • Caveolin 1 (links | edit)
  • STX1A (links | edit)
  • COPB1 (links | edit)
  • DNM2 (links | edit)
  • RAB3A (links | edit)
  • STX4 (links | edit)
  • SYT1 (links | edit)
  • Biogenesis of lysosome-related organelles complex 1 (links | edit)
  • CLTC (links | edit)
  • DNM1 (links | edit)
  • VAMP2 (links | edit)
  • LMAN1 (links | edit)
  • Perilipin-3 (links | edit)
  • STX7 (links | edit)
  • STX6 (links | edit)
  • COPE (gene) (links | edit)
  • AP3B1 (links | edit)
  • VAMP3 (links | edit)
  • STX5 (links | edit)
  • COPB2 (links | edit)
  • STX2 (links | edit)
  • COPG2 (links | edit)
  • COPG (links | edit)
  • STX12 (links | edit)
  • STX8 (links | edit)
  • Syntaxin binding protein 2 (links | edit)
  • DNM3 (links | edit)
  • AP1S2 (links | edit)
  • SNAP29 (links | edit)
  • SYT2 (links | edit)
  • SYT3 (links | edit)
  • SYT9 (links | edit)
  • VAMP1 (links | edit)
  • STX16 (links | edit)
  • SYT11 (links | edit)
  • VPS33B (links | edit)
  • SYT5 (links | edit)
  • SYT13 (links | edit)
  • SYT4 (links | edit)
  • SYT7 (links | edit)
  • COPZ1 (links | edit)
  • SEC24C (links | edit)
  • Caveolin 2 (links | edit)
  • SYT6 (links | edit)
  • STX1B (links | edit)
  • X-linked intellectual disability (links | edit)
  • Congenital generalized lipodystrophy (links | edit)
  • Syntaxin 3 (links | edit)
  • Syntaxin (links | edit)
  • Sorting nexin (links | edit)
  • Arthrogryposis–renal dysfunction–cholestasis syndrome (links | edit)
  • CEDNIK syndrome (links | edit)
  • Munc-18 (links | edit)
  • Cranio-lenticulo-sutural dysplasia (links | edit)
  • Inherited disorders of trafficking (links | edit)
  • Vacuolar protein sorting (links | edit)
  • List of OMIM disorder codes (links | edit)
  • Active zone (links | edit)
  • SEC24A (links | edit)
  • Clathrin adaptor protein (links | edit)
  • Biogenesis of lysosome-related organelles complex 3 (links | edit)
  • List of human protein-coding genes 3 (links | edit)
  • Halperin-Birk syndrome (links | edit)
  • Talk:SEC23A (links | edit)
  • User:ProteinBoxBot/PBB Log Wiki 12-24-2007-A-26 (links | edit)
  • User:AlexNewArtBot/TestFeedSearchResult/archive27 (links | edit)
  • User:ProteinBoxBot/Protein Directory links (links | edit)
  • User:Andrew Su/Interactions (links | edit)
  • User:NussPoyava/sandbox (links | edit)
  • User:MKClement/proposal/draft (links | edit)
  • User:Mcb200 2014/sandbox (links | edit)
  • User:KadaneBot/Task3/Edits/gene/Case 1/1 (links | edit)
  • User:Seppi333/GeneListNLP (links | edit)
  • User:NuriHalperin/sandbox (links | edit)
  • User talk:X!/Archives/5/2011 (links | edit)
  • Template:Vesicular transport proteins (links | edit)
  • Template:Vesicular transport protein disorders (links | edit)
• CLN8 (links | edit)
• SYT9 (links | edit)
• VAMP1 (links | edit)
• STX16 (links | edit)
• SYT11 (links | edit)
• VPS33B (links | edit)
• SYT5 (links | edit)
• SYT13 (links | edit)
• SYT4 (links | edit)
• SYT7 (links | edit)