CD59 wt Allele

Preferred Label : CD59 wt Allele;

NCIt synonyms : HRF20; 16.3A5; EJ16; CD59 Molecule, Complement Regulatory Protein wt Allele; Human Leukocyte Antigen MIC11 Gene; p18-20; MIC11; MIN3; EJ30; MIN2; 1F5; MACIF; G344; FLJ38134; MIN1; MSK21; EL32; Lymphocytic Antigen CD59/MEM43 Gene; MAC-IP; MIRL; MGC2354; MEM43; FLJ92039; CD59 Antigen p18-20 (Antigen Identified by Monoclonal Antibodies 16.3A5, EJ16, EJ30, EL32 and G344) Gene; HRF-20; CD59 Molecule (CD59 Blood Group) wt Allele; Surface Antigen Identified by Monoclonal Antibody 16.3A5 Gene;

NCIt definition : Human CD59 wild-type allele is located in the vicinity of 11p13 and is approximately 33 kb in length. This allele, which encodes CD59 glycoprotein, plays a role in the negative regulation of the complement cascade. Mutation of the gene is associated with CD59 deficiency.;

GenBank Accession Number : NM_203329;

Details

Origin ID

C95933;

UMLS CUI

C3272448;

Automatic exact mappings (from CISMeF team)
- CD59 Antigens [MeSH Descriptor]
- CD59 molecule (CD59 blood group) [ORDO Gene]
- Cd59 antigen [OMIM gene]
OMIM relation
- Cd59 antigen [OMIM gene]
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
- 11p13 [NCIt concept]
gene_is_element_in_pathway
- Complement and Coagulation Cascade [NCIt concept]
- Hematopoietic Cell Lineage Pathway [NCIt concept]
gene_plays_role_in_process
- Negative Regulation of Complement Activation [NCIt concept]

Keyword's position in hierarchy(ies) :

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