AlphaFold predicted structure
PEX26 · Q7Z412


Mean pLDDT
79.5/ 100
Confident
305 residues
Confidence breakdown
- Very high(≥ 90)48%
- Confident(70–90)23%
- Low(50–70)16%
- Very low(< 50)13%
AlphaFold (Jumper et al., 2021) · CC BY 4.0
peroxisomal biogenesis factor 26
Annotations refreshed 1 month ago.
Diagnostic Grade (Green)
Adult onset leukodystrophy
BIALLELIC, autosomal or pseudoautosomalAmelogenesis imperfecta
BIALLELIC, autosomal or pseudoautosomalArthrogryposis
BIALLELIC, autosomal or pseudoautosomalBilateral congenital or childhood onset cataracts
BIALLELIC, autosomal or pseudoautosomalCholestasis
BIALLELIC, autosomal or pseudoautosomalDDG2P
BIALLELIC, autosomal or pseudoautosomalFetal anomalies
BIALLELIC, autosomal or pseudoautosomalFetal hydrops
BIALLELIC, autosomal or pseudoautosomal+11 more panels — install the extension to see the full list inline on any page.
Peroxisome biogenesis disorder-Zellweger syndrome spectrum
peroxisome biogenesis disorder 7A (Zellweger)
Zellweger syndrome
peroxisome biogenesis disorder
Zellweger spectrum disorders
peroxisomal disease
peroxisome biogenesis disorder 1A (Zellweger)
amelogenesis imperfecta
peroxisome biogenesis disorder type 3B
peroxisome biogenesis disorder 2B
Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.
Peroxisome assembly protein 26
Peroxisomal docking factor that anchors PEX1 and PEX6 to peroxisome membranes (PubMed:12717447, PubMed:12851857, PubMed:16257970, PubMed:16763195, PubMed:16854980, PubMed:21362118). PEX26 is therefore required for the formation of the PEX1-PEX6 AAA ATPase complex, a complex that mediates the extraction of the PEX5 receptor from peroxisomal membrane (PubMed:12717447, PubMed:12851857, PubMed:16257970, PubMed:16763195, PubMed:16854980, PubMed:21362118)
PEX26 · Q7Z412


Mean pLDDT
79.5/ 100
Confident
305 residues
Confidence breakdown
AlphaFold (Jumper et al., 2021) · CC BY 4.0