Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 9409
MIM: 603360
HGNC: 8857
Ensembl: ENSG00000121680
Variants:
dbSNP: 9409
ClinVar: 9409
TCGA: ENSG00000121680
COSMIC: PEX16
RNA/Proteins
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Peroxisome | KEGG | ko04146 |
| Peroxisome | KEGG | hsa04146 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34360754 | 2021 | Knockdown of PEX16 Induces Autophagic Degradation of Peroxisomes. | 1 |
| 34360754 | 2021 | Knockdown of PEX16 Induces Autophagic Degradation of Peroxisomes. | 1 |
| 25002403 | 2014 | PEX16 contributes to peroxisome maintenance by constantly trafficking PEX3 via the ER. | 23 |
| 25002403 | 2014 | PEX16 contributes to peroxisome maintenance by constantly trafficking PEX3 via the ER. | 23 |
| 21768384 | 2011 | Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells. | 37 |
| 21768384 | 2011 | Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells. | 37 |
| 20647552 | 2010 | Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene. | 31 |
| 20647552 | 2010 | Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene. | 31 |
| 16717127 | 2006 | The origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER. | 140 |
| 16717127 | 2006 | The origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER. | 140 |
| 11890679 | 2002 | A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome. | 2 |
| 12223482 | 2002 | The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly. | 22 |
| 11890679 | 2002 | A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome. | 2 |
| 12223482 | 2002 | The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly. | 22 |
Citation
Dessen P
PEX16 (peroxisomal biogenesis factor 16)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/71838/cancer-prone-explorer/new-content/
