MOG wt Allele - CISMeF

Preferred Label : MOG wt Allele;

NCIt synonyms : MOGIG2; BTNL11; NRCLP7; BTN6; Myelin Oligodendrocyte Glycoprotein wt Allele; MOG AluB Gene; MOG AluA Gene; MOG Ig-AluB Gene; MOG Alpha-5 Gene;

NCIt definition : Human MOG wild-type allele is located in the vicinity of 6p22.1 and is approximately 15 kb in length. This allele, which encodes myelin-oligodendrocyte glycoprotein, is involved in cell-cell communication and myelin sheath formation and maintenance. Mutation of the gene is associated with narcolepsy and cataplexy (narcolepsy type 7).;

GenBank Accession Number : NM_002433;

Details

Origin ID

C200638;

OMIM relation
- Myelin-oligodendrocyte glycoprotein [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 6p22.1 [NCIt concept]
gene_plays_role_in_process
- Cell Adhesion Process [NCIt concept]
- Cell-Cell Adhesion Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Protein-Carbohydrate Interaction [NCIt concept]
- Receptor Signaling [NCIt concept]

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