Search Ontology:
ChEBI
CID 91856002
- Term ID
- CHEBI:148487
- Synonyms
-
- NeuAc(a2-3)Gal(b1-4)GlcNAc(b1-2)[NeuAc(a2-3)Gal(b1-3)[NeuAc(a2-6)]GlcNAc(b1-4)]Man(a1-3)[NeuAc(a2-3)Gal(b1-4)GlcNAc(b1-2)Man(a1-6)]Man(b1-4)GlcNAc(b1-4)GlcNAc
- WURCS=2.0/6,15,14/[a2122h-1x_1-5_2*NCC/3=O][a2122h-1b_1-5_2*NCC/3=O][a1122h-1b_1-5][a1122h-1a_1-5][a2112h-1b_1-5][Aad21122h-2a_2-6_5*NCC/3=O]/1-2-3-4-2-5-6-2-5-6-6-4-2-5-6/a4-b1_b4-c1_c3-d1_c6-l1_d2-e1_d4-h1_e4-f1_f3-g2_h3-i1_h6-k2_i3-j2_l2-m1_m4-n1_n3-o2
- Definition
- References
-
- GlyGen:G22732WO
- GlyTouCan:G22732WO
- Ontology
- ChEBI ( EBI )
Phenotype
Phenotype resulting from CID 91856002
Phenotype where environments contain CID 91856002
Phenotype modified by environments containing CID 91856002
Phenotype affecting CID 91856002
Human Disease Model