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FLASH GENE
Symbol PEX16 contributors: mct - updated : 05-09-2014
HGNC name peroxisomal biogenesis factor 16
HGNC id 8857
Corresponding disease
PBD9 peroxisome biogenesis disorder 9, Zellweger spectrum
Location 11p11.2      Physical location : 45.931.220 - 45.939.674
Synonym symbol(s) HGNC8857
DNA
TYPE functioning gene
STRUCTURE 8.45 kb     11 Exon(s)
10 Kb 5' upstream gene genomic sequence study
MAPPING cloned Y linked N status provisional
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
11 splicing 1929 38 336 - 2006 16717127
11 - 1794 - 346 - 2006 16717127
EXPRESSION
Type restricted
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Digestiveintestinelarge intestinecolon highly
Endocrineneuroendocrinepituitary   
Reproductivefemale systemuteruscervix  
 female systembreastmammary gland  
Visualeye   highly
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
HOMOLOGY
interspecies ortholog to murine Pex16
homolog to dog LOC483639
Homologene
FAMILY
CATEGORY regulatory , structural protein
SUBCELLULAR LOCALIZATION     intracellular
intracellular,cytoplasm,organelle,membrane
intracellular,cytoplasm,organelle,peroxisome
intracellular,cytoplasm,organelle,endoplasmic reticulum
basic FUNCTION
  • playing a central role in peroxisomal membrane biogenesis, more likely updtream PEX3
  • implicated in the origin and maintenance of peroxisomes involving a de novo PEX16-dependent pathway from the Endoplasmic reticulum
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
  • PEX19
  • PEX3 requires PEX16 for ER location but is dispensable for the ER location of PEX16
  • SEC16B plays an important role in the transport of PEX16 from the ER to peroxisomes in mammalian cells
  • PEX16 mediates the peroxisomal trafficking of two distinct peroxisomal membrane proteins, PEX3 and SLC25A17, via the ER
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) PBD9
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS