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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060180 | colitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0050669 | spastic cerebral palsy | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:1596 | depressive disorder | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:700 | mitochondrial metabolism disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:10140 | dry eye syndrome | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:12858 | Huntington's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:5082 | liver cirrhosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0060585 | Noonan syndrome 7 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:13208 | background diabetic retinopathy | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:418 | systemic scleroderma | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:874 | bacterial pneumonia | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:5940 | malignant peripheral nerve sheath tumor | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:5844 | myocardial infarction | HGNC:2634 | Homo sapiens (human) | 1573 | CYP2J2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4242 | Homo sapiens (human) | 9945 | GFPT2 |
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| DOID:1508 | candidiasis | HGNC:4017 | Homo sapiens (human) | 2528 | FUT6 |
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| DOID:9269 | maple syrup urine disease | HGNC:987 | Homo sapiens (human) | 594 | BCKDHB |
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| DOID:9970 | obesity | HGNC:3569 | Homo sapiens (human) | 2180 | ACSL1 |
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| DOID:5082 | liver cirrhosis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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