Identity
HGNC
LOCATION
1p36.32
LOCUSID
ALIAS
NALD,PBD6A,PBD6B,RNF69
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: 5192
MIM: 602859
HGNC: 8851
Ensembl: ENSG00000157911
Variants:
dbSNP: 5192
ClinVar: 5192
TCGA: ENSG00000157911
COSMIC: PEX10
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 |
|---|---|---|---|
| 33784440 | 2021 | Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort. | 9 |
| 33784440 | 2021 | Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort. | 9 |
| 30863997 | 2019 | PEX10, SIRPA-SIRPG, and SOX5 gene polymorphisms are strongly associated with nonobstructive azoospermia susceptibility. | 12 |
| 30863997 | 2019 | PEX10, SIRPA-SIRPG, and SOX5 gene polymorphisms are strongly associated with nonobstructive azoospermia susceptibility. | 12 |
| 27230853 | 2016 | Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia. | 5 |
| 27230853 | 2016 | Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia. | 5 |
| 25636090 | 2015 | [Abnormal expression of PEX10 gene may be related to epilepsy associated with 1p36 copy number variations]. | 0 |
| 25636090 | 2015 | [Abnormal expression of PEX10 gene may be related to epilepsy associated with 1p36 copy number variations]. | 0 |
| 20695019 | 2010 | Mutations in PEX10 are a cause of autosomal recessive ataxia. | 25 |
| 20695019 | 2010 | Mutations in PEX10 are a cause of autosomal recessive ataxia. | 25 |
| 19105186 | 2009 | Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders. | 31 |
| 19105186 | 2009 | Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders. | 31 |
| 14713216 | 2003 | Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. | 3 |
| 14713216 | 2003 | Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. | 3 |
Citation
Dessen P
PEX10 (peroxisomal biogenesis factor 10)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/71832/new-content/tumors-explorer/
