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- Table of Contents
Facts about Peroxisome biogenesis factor 10.
Human | |
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Gene Name: | PEX10 |
Uniprot: | O60683 |
Entrez: | 5192 |
Belongs to: |
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pex2/pex10/pex12 family |
NALD; peroxin 10; peroxin-10; peroxisomal biogenesis factor 10MGC1998; Peroxisome assembly protein 10; RING finger protein 69; RNF69peroxisome biogenesis factor 10
Mass (kDA):
37.069 kDA
Human | |
---|---|
Location: | 1p36.32 |
Sequence: | 1; NC_000001.11 (2403974..2413827, complement) |
Peroxisome membrane; Peripheral membrane protein.
PMID: 9683594 by Warren D.S., et al. Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.
PMID: 9700193 by Okumoto K., et al. Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.