Functional category : Peroxisome biogenesis (peroxins)

Name : Peroxisome biogenesis (peroxins)
Organism : Pan troglodytes
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
ENSPTRG00000014046
ENSPTRG00000000132
ENSPTRG00000000050
ENSPTRG00000020359
ENSPTRG00000004610
ENSPTRG00000011952
ENSPTRG00000014045
ENSPTRG00000001203
ENSPTRG00000011953
ENSPTRG00000018179
PEX1
PEX11A
PEX11G
PEX12
PEX16
PEX3
PEX5L
PEX7
Disease(s) :
Image(s) :

[top] Image description : Peroxins and other PMPs

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