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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:8634 | prostate carcinoma in situ | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:9884 | muscular dystrophy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2018 | hyperinsulinism | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:8741 | seborrheic dermatitis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:11121 | pulpitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:1574 | alcohol use disorder | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:0080158 | herpes simplex virus keratitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0080108 | myoglobinuria | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:841 | extrinsic allergic alveolitis | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:9252 | amino acid metabolic disorder | HGNC:5005 | Homo sapiens (human) | 3155 | HMGCL |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:2216 | factor V deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:10591 | pre-eclampsia | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:2377 | multiple sclerosis | HGNC:928 | Homo sapiens (human) | 9334 | B4GALT5 |
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| DOID:3770 | pulmonary fibrosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:8947 | diabetic retinopathy | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:7148 | rheumatoid arthritis | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:2841 | asthma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050453 | lissencephaly | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:0050709 | early infantile epileptic encephalopathy | HGNC:5386 | Homo sapiens (human) | 3421 | IDH3G |
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| DOID:5082 | liver cirrhosis | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:11476 | osteoporosis | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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