FBXO38 wt Allele

Preferred Label : FBXO38 wt Allele;

NCIt synonyms : FLJ13962; MOKA; Modulator of Klf7 Activity, Mouse, Homolog of Gene; HMN2D; SP329; F-Box Protein 38 wt Allele; Fbx38;

NCIt definition : Human FBXO38 wild-type allele is located in the vicinity of 5q32 and is approximately 59 kb in length. This allele, which encodes F-box only protein 38, may be involved in protein ubiquitination.;

NCIt note : There is a report of a chromosomal aberration involving the AGT4C gene and the FBXO38 gene, which is associated with breast cancer. (COSMIC);

GenBank Accession Number : BC005873;

Details

Origin ID

C114611;

UMLS CUI

C3889143;

Automatic exact mappings (from CISMeF team)
- F-box only protein 38 [OMIM gene]
- F-box protein 38 [ORDO Gene]
- Neuronopathy, distal hereditary motor, autosomal dominant 6 [OMIM Phenotype]
OMIM relation
- F-box only protein 38 [OMIM gene]
See also inter- (CISMeF)
- distal hereditary motor neuronopathy type 2D [DO Concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 5q32 [NCIt concept]

Keyword's position in hierarchy(ies) :

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