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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:0060108 | brain glioma | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:10825 | essential hypertension | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:9408 | acute myocardial infarction | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:9970 | obesity | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:0050753 | cerebellar ataxia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1227 | neutropenia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0050700 | cardiomyopathy | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:9351 | diabetes mellitus | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0060867 | macrocephaly-autism syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:2841 | asthma | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:13608 | biliary atresia | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0081267 | graft-versus-host disease | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:3459 | breast carcinoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:0050083 | Keshan disease | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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| DOID:4483 | rhinitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:4362 | cervical cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | HGNC:4125 | Homo sapiens (human) | 2591 | GALNT3 |
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| DOID:11446 | sciatic neuropathy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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