PEX10
Sign in to saveAlso known as NALD, PBD6A, PBD6B, RNF69, peroxisomal biogenesis factor 10
Peroxisome biogenesis factor 10 is a protein that in humans is encoded by the PEX10 gene. Alternative splicing results in two transcript variants encoding different isoforms.
Gene data
PEX10- Name
- peroxisomal biogenesis factor 10
- Type
- protein-coding
- Aliases
- NALD, PBD6A, PBD6B, RNF69
This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008].
via MyGene.info
Gene · Ensembl
peroxisomal biogenesis factor 10
- Symbol
- PEX10
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 1:2,403,784-2,413,797
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- exact match
- identifiers.org/ncbigene/5192
- HomoloGene ID
- 5671
- genomic end
- 2345236
- genomic start
- 2336236
- cytogenetic location
- 1p36.32
via Wikidata · CC0
~1 min read
Article
6 sectionsContents
- Function
- Clinical significance
- Interactions
- References
- Further reading
- External links
Peroxisome biogenesis factor 10 is a protein that in humans is encoded by the PEX10 gene. Alternative splicing results in two transcript variants encoding different isoforms.
== Function ==