PEX13 Proteine (PEX13)

This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome.

• Peroxin 13 (Pex13)
• peroxisomal biogenesis factor 13 (Pex13)
• peroxisomal biogenesis factor 13 (pex13)
• peroxisomal biogenesis factor 13 (PEX13)
• peroxin PEX13 (PEX13)
• Alle Gen-Bezeichnungen
• peroxin 13 (predicted) (pex13)
• peroxin (PEX13)
• SH3 domain-containing protein (pex13)
• putative peroxin 13 (PEX13)
• peroxisome biogenesis factor 13 (pex13)

• 2610008O20Rik Protein
• CG4663 Protein
• DDBDRAFT_0191662 Protein
• DDBDRAFT_0238077 Protein
• DDB_0191662 Protein
• Alle Synonyme
• DDB_0238077 Protein
• DmelPex13 Protein
• Dmel\\CG4663 Protein
• NALD Protein
• PAS20 Protein
• PBD11A Protein
• PBD11B Protein
• pex13 Protein
• zgc:66124 Protein
• ZWS Protein

CG4663-PA , Pex13-PA , peroxin 13 , peroxisomal membrane protein PEX13 , peroxisome biogenesis factor 13 , peroxin-13 , potential peroxisomal membrane protein Pex13 , peroxisomal biogenesis factor 13 , transmembrane protein , putative peroxin 13 , Peroxisomal membrane protein PEX13 , peroxisomal membrane protein PEX13-like