Identity
HGNC
LOCATION
2p15
LOCUSID
ALIAS
NALD,PBD11A,PBD11B,ZWS
FUSION GENES
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: 5194
MIM: 601789
HGNC: 8855
Ensembl: ENSG00000162928
Variants:
dbSNP: 5194
ClinVar: 5194
TCGA: ENSG00000162928
COSMIC: PEX13
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000162928 | ENST00000295030 | Q92968 |
| ENSG00000162928 | ENST00000401576 | B5MBY9 |
| ENSG00000162928 | ENST00000414712 | G5E9N6 |
| ENSG00000162928 | ENST00000444100 | D3YTD3 |
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Peroxisome | KEGG | ko04146 |
| Peroxisome | KEGG | hsa04146 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38632234 | 2024 | Modulation of peroxisomal import by the PEX13 SH3 domain and a proximal FxxxF binding motif. | 0 |
| 38632234 | 2024 | Modulation of peroxisomal import by the PEX13 SH3 domain and a proximal FxxxF binding motif. | 0 |
| 35854306 | 2022 | Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders. | 2 |
| 35854306 | 2022 | Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders. | 2 |
| 32565019 | 2020 | Hepatocyte-specific deletion of peroxisomal protein PEX13 results in disrupted iron homeostasis. | 2 |
| 32565019 | 2020 | Hepatocyte-specific deletion of peroxisomal protein PEX13 results in disrupted iron homeostasis. | 2 |
| 27827795 | 2017 | Peroxisomal protein PEX13 functions in selective autophagy. | 26 |
| 28765278 | 2017 | The peroxisomal matrix protein translocon is a large cavity-forming protein assembly into which PEX5 protein enters to release its cargo. | 13 |
| 27827795 | 2017 | Peroxisomal protein PEX13 functions in selective autophagy. | 26 |
| 28765278 | 2017 | The peroxisomal matrix protein translocon is a large cavity-forming protein assembly into which PEX5 protein enters to release its cargo. | 13 |
| 23716570 | 2013 | Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis. | 14 |
| 23716570 | 2013 | Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis. | 14 |
| 19449432 | 2009 | Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations. | 7 |
| 19449432 | 2009 | Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations. | 7 |
| 16006427 | 2005 | Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder. | 4 |
Citation
Dessen P
PEX13 (peroxisomal biogenesis factor 13)
Atlas Genet Cytogenet Oncol Haematol. 2017-10-01
Online version: http://atlasgeneticsoncology.org/gene/57179/pex13-(peroxisomal-biogenesis-factor-13)
