PEX26 wt Allele

Preferred Label : PEX26 wt Allele;

NCIt synonyms : FLJ20695; Peroxisome Biogenesis Disorder, Complementation Group A Gene; Peroxisome Biogenesis Factor 26 Gene; Peroxisome Biogenesis Disorder, Complementation Group 8 Gene; Peroxin 26 Gene; PBD7A; Peroxisomal Biogenesis Factor 26 wt Allele; PBD7B; Pex26pM1T; PEX26M1T;

NCIt definition : Human PEX26 wild-type allele is located in the vicinity of 22q11.21 and is approximately 27 kb in length. This allele, which encodes peroxisome assembly protein 26, plays a role in the localization of PEX1-PEX6 AAA ATPase complex. Mutation of the gene is associated with peroxisomal biogenesis disorder types 7A and 7B.;

NCI Metathesaurus CUI : CL1926570;

GenBank Accession Number : AB089678;

Details

Origin ID

C204449;

UMLS CUI

C5890952;

OMIM relation
- Peroxisome biogenesis factor 26 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 22q11.21 [NCIt concept]
gene_is_element_in_pathway
- Peroxisome Biogenesis Pathway [NCIt concept]
gene_plays_role_in_process
- Cellular Stress Response [NCIt concept]
- Intracellular Transport [NCIt concept]
- Ligand Binding [NCIt concept]
- Subcellular Protein Targeting [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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