FAF2 wt Allele

Preferred Label : FAF2 wt Allele;

NCIt synonyms : Expressed In T Cells and Eosinophils In Atopic Dermatitis 2 Gene; UBXN3B; Expressed In T-Cells and Eosinophils In Atopic Dermatitis Gene; FAF Family, Member 2 Gene; UBXD8; Fas-Associated Factor Family, Member 2 Gene; KIAA0887; Fas Associated Factor Family Member 2 wt Allele; ETEA;

NCIt definition : Human FAF2 wild-type allele is located in the vicinity of 5q35.2 and is approximately 62 kb in length. This allele, which encodes FAS-associated factor 2 protein, plays a role in endoplasmic reticulum-associated degradation of misfolded proteins and the regulation of apoptosis. Aberrant overexpression of the gene is associated with atopic dermatitis.;

NCI Metathesaurus CUI : CL1648382;

GenBank Accession Number : BC015791;

Details

Origin ID

C179138;

UMLS CUI

C5551110;

Automatic exact mappings (from CISMeF team)
- Fas-associated factor family, member 2 [OMIM gene]
OMIM relation
- Fas-associated factor family, member 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 5q35.2 [NCIt concept]
gene_plays_role_in_process
- Protein Turnover [NCIt concept]
- Ubiquitinated Protein Degradation [NCIt concept]
- Unfolded Protein Response [NCIt concept]

Keyword's position in hierarchy(ies) :

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