Functional category : Peroxisome biogenesis (peroxins)

Name : Peroxisome biogenesis (peroxins)
Organism : Debaryomyces hansenii
Description : Essential peroxisomal proteins involved in the biogenesis of the peroxisome. Their loss of function abrogates the organelle formation, causing severe human diseases: Zellweger syndrome, neonatal adrenoleukodystrophy, infantile Refsum disease or rhizomelic chondrodysplasia punctata type 1.
Gene(s) :
GENE PROTEIN FAMILY
DEHA0A01683g
DEHA0A05918g
DEHA0A07260g
DEHA0A11781g
DEHA0B03894g
DEHA0B08767g
DEHA0C05720g
DEHA0C14388g
DEHA0D12166g
DEHA0D13057g
DEHA0D15444g
DEHA0E08701g
DEHA0E15785g
DEHA0F01595g
DEHA0F10021g
DEHA0F10087g
DEHA0F23133g
DEHA0F27577g
DEHA0G12639g
DEHA0G18161g
DEHA0G23782g
Disease(s) :
Image(s) :

[top] Image description : Peroxins and other PMPs

Peroxins and other PMPs
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Peroxins-and-other-PMPs.jpg