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PEX13

Official Full Name
peroxisomal biogenesis factor 13
Organism
Homo sapiens
GeneID
5194
Background
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. [provided by RefSeq, Oct 2008]
Synonyms
ZWS; NALD; PBD11A; PBD11B;

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