PEX7
Identifiers
Aliases	PEX7, PBD9B, PTS2R, RCDP1, RD, peroxisomal biogenesis factor 7
External IDs	OMIM: 601757; MGI: 1321392; GeneCards: PEX7
Gene location (Human) Chr. Chromosome 6 (human)[1] Band 6q23.3 Start 136,822,564 bp[1] End 136,913,934 bp[1]
Gene location (Mouse) Chr. Chromosome 10 (mouse)[2] Band 10|10 A3 Start 19,729,646 bp[2] End 19,783,435 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in retinal pigment epithelium sperm right adrenal gland right adrenal cortex left adrenal gland secondary oocyte gonad body of pancreas left adrenal cortex kidney tubule Top expressed in left lobe of liver right kidney right ventricle triceps brachii muscle spermatocyte proximal tubule sternocleidomastoid muscle epithelium of stomach pyloric antrum brown adipose tissue More reference expression data BioGPS n/a
Gene ontology Molecular function enzyme binding peroxisome matrix targeting signal-2 binding protein homodimerization activity Cellular component cytoplasm peroxisome peroxisomal matrix peroxisomal membrane cytosol Biological process protein transport fatty acid beta-oxidation peroxisome organization neuron migration protein import into peroxisome matrix endochondral ossification ether lipid biosynthetic process protein targeting to peroxisome Sources:Amigo / QuickGO
Orthologs Databases NCBI: entry; OMA: entry Species Human Mouse Entrez 5191 18634 Ensembl ENSG00000112357 ENSMUSG00000020003 UniProt O00628 P97865 RefSeq (mRNA) NM_000288 NM_001161825 NM_008822 RefSeq (protein) NP_000279 NP_001155297 NP_032848 Location (UCSC) Chr 6: 136.82 – 136.91 Mb Chr 10: 19.73 – 19.78 Mb PubMed search [3] [4]
Wikidata
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Peroxin-7 is a receptor associated with Refsum's disease and rhizomelic chondrodysplasia punctata type 1. Peroxin-7 is encoded in humans by the PEX7 gene.

See also

• Peroxin

References

External links

• GeneReviews/NCBI/NIH/UW entry on Refsum Disease
• GeneReviews/NIH/NCBI/UW entry on Rhizomelic Chondrodysplasia Punctata Type 1
• PEX7+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

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