Pathway Name | Organism |
---|---|
APAP ADME | Homo sapiens |
Aspirin ADME | Homo sapiens |
Defective UGT1A1 causes hyperbilirubinemia | Homo sapiens |
Glucuronidation | Homo sapiens |
Heme degradation | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
DOID:0090104 | Huntington's disease-like 2 | |
DOID:0110029 | alpha thalassemia-intellectual disability syndrome type 1 | |
DOID:0110030 | alpha thalassemia-X-linked intellectual disability syndrome | |
DOID:0110031 | hemoglobin H disease | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 | |
DOID:0110038 | Alzheimer's disease 6 | |
DOID:0110039 | Alzheimer's disease 7 | |
DOID:0110041 | Alzheimer's disease 8 | |
DOID:0110043 | Alzheimer's disease 10 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024