PEX13
Sign in to saveAlso known as NALD, PBD11A, PBD11B, ZWS, peroxisomal biogenesis factor 13
Gen der Spezies Homo sapiens
Gene data
PEX13- Name
- peroxisomal biogenesis factor 13
- Type
- protein-coding
- Position
- 61,017,058–61,062,516 (+)
- Aliases
- NALD, PBD11A, PBD11B, ZWS
- Ensembl
- ENSG00000162928
- RefSeq RNA
- NM_002618.4
- RefSeq protein
- NP_002609.1
This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008].
Gene Ontology
Biological process
Molecular function
Pathways
Peroxisome - Homo sapiens (human)Metabolism of proteinsPost-translational protein modificationProtein ubiquitinationE3 ubiquitin ligases ubiquitinate target proteinsPeroxisomal protein importPeroxisomal protein importClass I peroxisomal membrane protein importProtein localizationProtein localization
via MyGene.info
Gene · Ensembl
peroxisomal biogenesis factor 13
- Symbol
- PEX13
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 2:61,017,058-61,062,516
- Strand
- Forward (+)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- Protein PEX13 PDB 1wxu.png
Show 8 more facts
- HomoloGene ID
- 1967
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/5194
- genomic end
- 61279125
- genomic start
- 61244360
- chromosome
- human chromosome 2
- cytogenetic location
- 2p15
- genetic association
- Zellweger syndrome
via Wikidata · CC0