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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:5419 | schizophrenia | HGNC:6825 | Homo sapiens (human) | 4122 | MAN2A2 |
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| DOID:4989 | pancreatitis | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:10283 | prostate cancer | HGNC:785 | Homo sapiens (human) | 467 | ATF3 |
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| DOID:12336 | male infertility | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050850 | diabetic encephalopathy | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:399 | tuberculosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:11168 | anogenital venereal wart | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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| DOID:13001 | carotid stenosis | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:162 | cancer | HGNC:8995 | Homo sapiens (human) | 8395 | PIP5K1B |
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| DOID:1701 | steroid inherited metabolic disorder | HGNC:5215 | Homo sapiens (human) | 51478 | HSD17B7 |
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| DOID:1059 | intellectual disability | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:2841 | asthma | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:3312 | bipolar disorder | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:2349 | arteriosclerosis | HGNC:405 | Homo sapiens (human) | 218 | ALDH3A1 |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:12401 | intermittent explosive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:1679 | cystitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1520 | colon carcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0112222 | developmental and epileptic encephalopathy 88 | HGNC:6970 | Homo sapiens (human) | 4190 | MDH1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:11702 | dysgammaglobulinemia | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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