PEX7

gene product
PTS2R, RD
This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq, Oct 2008]
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35 antibodies from 12 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
antibodies-online
13 antibodies
Novus Biologicals
4 antibodies
Proteintech Group
1 antibody
LifeSpan BioSciences, Inc.
5 antibodies
EMD Millipore
1 antibody
Abnova Corporation
1 antibody
Aviva Systems Biology
2 antibodies
Atlas Antibodies
1 antibody
GeneTex
1 antibody
Creative Biomart
3 antibodies
RabMAbs
2 antibodies
Sigma-Aldrich
1 antibody