Search Ontology:
ChEBI
CID 91848175
- Term ID
- CHEBI:153609
- Synonyms
-
- NeuAc(a2-6)Gal(b1-4)GlcNAc(b1-3)Gal(b1-4)GlcNAc(b1-3)Gal(b1-4)GlcNAc(b1-2)[Fuc(a1-3)[Gal(b1-4)]GlcNAc(b1-3)Gal(b1-4)[Fuc(a1-3)]GlcNAc(b1-3)Gal(b1-4)[Fuc(a1-3)]GlcNAc(b1-4)]Man(a1-3)[NeuAc(a2-3)Gal(b1-4)[Fuc(a1-3)]GlcNAc(b1-3)Gal(b1-4)[Fuc(a1-3)]GlcNAc(b1-
- WURCS=2.0/7,37,36/[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][a1221m-1a_1-5]/1-2-3-4-2-5-2-5-2-5-6-2-7-5-2-7-5-2-7-5-4-2-5-2-5-2-5-2-5-2-7-5-2-7-5-6-7/a4-b1_a6-K1_b4-c1_c3-d1_
- Definition
- References
-
- GlyGen:G76705YY
- GlyTouCan:G76705YY
- Ontology
- ChEBI ( EBI )
Phenotype
Phenotype resulting from CID 91848175
Phenotype where environments contain CID 91848175
Phenotype modified by environments containing CID 91848175
Phenotype affecting CID 91848175
Human Disease Model