PEX10

Name

peroxisomal biogenesis factor 10

Type

protein-coding

Position

2,403,784–2,413,797 (−)

Aliases

NALD, PBD6A, PBD6B, RNF69

Ensembl

ENSG00000157911

RefSeq RNA

NM_001374425.1, NM_001374426.1, NM_001374427.1, NM_002617.4, NM_153818.2

RefSeq protein

NP_001361354.1, NP_001361355.1, NP_001361356.1, NP_002608.1, NP_722540.1

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

Wikidata facts

Instance of

gene

via Wikidata · CC0