PEX16 Products

Description

The protein encoded by the PEX16 gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described. [provided by RefSeq]

Bioinformatics

Uniprot	AAH00467 Human AAH00467.1 Human NM_004813 Human NM_057174 Human NP_004804.1 Human Q9Y5Y5 Human
Product By Gene ID	9409
Alternate Names	Peroxin-16 peroxin-16 peroxisomal biogenesis factor 16peroxin 16 peroxisomal membrane protein PEX16 peroxisome biogenesis factor 16

Diseases related to PEX16

Discover more about diseases related to PEX16.

Zellweger Syndrome
Disorders Of Peroxisome Biogenesis
Peroxisomal Disorders
Muscle Hypotonia
Chondrodysplasia Punctata
Inborn Errors Of Metabolism
Ataxia
Neuronal Migration Disorders
Paraparesis
Refsum Disease
Cerebrovascular Accident
Chondrodysplasia Punctata, Rhizomelic
Potocki-shaffer Syndrome
Chronic Fatigue Syndrome
Hereditary Diseases

Pathways for PEX16

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Membrane Biogenesis
Protein Import
Localization
Transport
Membrane Assembly
Protein Secretion
Translation
Pathogenesis
Secretion
Cell Activation
Protein Targeting
T Cell Activation
Proteolysis
Membrane Fission
Organelle Localization
Secretory Pathway
Vesicle Transport
Peroxisome Fission
Glycosylation
Fatty Acid Beta-oxidation

PTMs for PEX16

Learn more about PTMs related to PEX16.

Glycosylation
Oxidation
Prenylation

Bioinformatics Tool for PEX16

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