MGP Database

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MGP002240

Record overview

MGPD IDMGP002240
Gene ID5194
SpeciesHomo sapiens (Human)
Gene Nameperoxisomal biogenesis factor 13
Gene Symbol PEX13
SynonymsZWS; NALD; PBD11A; PBD11B;
Alternate namesperoxisome biogenesis factor 13; peroxin-13; peroxisomal membrane protein PEX13;
Chromosome2
Map Location2p16.1
SummaryThis 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]
OrthologsView orthologs and multiple alignments for PEX13

Proteins

peroxisome biogenesis factor 13
Refseq ID:NP_002609
Protein GI:4505723
UniProt ID:Q92968
mRNA ID:NM_002618
Length:403
RefSeq Status:
MASQPPPPPKPWETRRIPGAGPGPGPGPTFQSADLGPTLMTRPGQPALTRVPPPILPRPSQQTGSSSVNTFRPAYSSFSSGYGAYGNSFYGGYSPYSYGY
NGLGYNRLRVDDLPPSRFVQQAEESSRGAFQSIESIVHAFASVSMMMDATFSAVYNSFRAVLDVANHFSRLKIHFTKVFSAFALVRTIRYLYRRLQRMLG
LRRGSENEDLWAESEGTVACLGAEDRAATSAKSWPIFLFFAVILGGPYLIWKLLSTHSDEVTDSINWASGEDDHVVARAEYDFAAVSEEEISFRAGDMLN
LALKEQQPKVRGWLLASLDGQTTGLIPANYVKILGKRKGRKTVESSKVSKQQQSFTNPTLTKGATVADSLDEQEAAFESVFVETNKVPVAPDSIGKDGEK
QDL
 
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