EPHB6 wt Allele

Preferred Label : EPHB6 wt Allele;

NCIt synonyms : HEP; EPH Receptor B6 wt Allele;

NCIt definition : Human EPHB6 wild-type allele is located in the vicinity of 7q34 and is approximately 16 kb in length. This allele, which encodes ephrin type-B receptor 6, is involved in the modulation of ephrin-B signaling.;

NCI Metathesaurus CUI : CL551947;

GenBank Accession Number : D83492;

Details

Origin ID

C150224;

UMLS CUI

C4723683;

Automatic exact mappings (from CISMeF team)
- Ephrin receptor ephb6 [OMIM gene]
- HEP (body structure) [SNOMED CT concept]
- Hepatoerythropoietic porphyria [ORDO Disease]
- Porphyria cutanea tarda [OMIM Phenotype]
- heel [MeSH Descriptor]
OMIM relation
- Ephrin receptor ephb6 [OMIM gene]
See also inter- (CISMeF)
- Hepatoerythropoietic porphyria [ICD-11 More detail]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 7q34 [NCIt concept]
gene_is_element_in_pathway
- Axon Guidance Pathway [NCIt concept]
gene_plays_role_in_process
- Ligand Binding [NCIt concept]
- Receptor Signaling [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients