peroxisome biogenesis factor 10; peroxin-10; peroxisome assembly protein 10; peroxisomal biogenesis factor 10; RING finger protein 69 (PEX10, RNF69)
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Function
- somewhat implicated in the biogenesis of peroxisomes
- interacts with PEX19
Structure
- belongs to the pex2/pex10/pex12 family
- contains 1 RING-type Zn+2 finger
Compartment
peroxisome membrane
Alternative splicing
named isoforms=2
Pathology
- defects in PEX10 are the cause of peroxisome biogenesis disorder complementation group 7
- defects in PEX10 are a cause of
More general terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/O60683.html
- ↑ GeneReviews https://www.genecards.org/cgi-bin/carddisp.pl?gene=PEX10
- ↑ dbPEX, PEX gene Database http://www.dbpex.org/home.php?select_db=PEX10
Database
- Entrez gene: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=5192
- Kegg: http://www.genome.jp/dbget-bin/www_bget?hsa:5192
- OMIM: https://mirror.omim.org/entry/202370
- OMIM: https://mirror.omim.org/entry/214100
- OMIM: https://mirror.omim.org/entry/601539
- OMIM: https://mirror.omim.org/entry/602859
- UniProt: http://www.uniprot.org/uniprot/O60683.html