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Peroxin-7

Family of transport proteins From Wikipedia, the free encyclopedia

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.

AliasesPEX7, PBD9B, PTS2R, RCDP1, RD, peroxisomal biogenesis factor 7
External IDsOMIM: 601757; MGI: 1321392; GeneCards: PEX7
End136,913,934 bp[1]
Quick facts PEX7, Identifiers ...
PEX7
Identifiers
AliasesPEX7, PBD9B, PTS2R, RCDP1, RD, peroxisomal biogenesis factor 7
External IDsOMIM: 601757; MGI: 1321392; GeneCards: PEX7
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000288

NM_001161825
NM_008822

RefSeq (protein)

NP_000279

NP_001155297
NP_032848

Location (UCSC)Chr 6: 136.82 – 136.91 MbChr 10: 19.73 – 19.78 Mb
PubMed search[3][4]
Wikidata
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Quick facts peroxisomal biogenesis factor 7, Identifiers ...
peroxisomal biogenesis factor 7
Identifiers
SymbolPEX7
NCBI gene5191
HGNC8860
OMIM601757
RefSeqNM_000288
UniProtO00628
Other data
LocusChr. 6 q21-q22.2
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StructuresSwiss-model
DomainsInterPro
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