PEX13
Sign in to saveAlso known as NALD, PBD11A, PBD11B, ZWS, peroxisomal biogenesis factor 13
Gen der Spezies Homo sapiens
In the Vinony graph
Within Vinony's link graph, PEX13 is referenced by 26 other articles, and connects out to PubMed, human chromosome 2 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 2.
Its subject is documented across 6 Wikipedia language editions.
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
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
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