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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:2986 | IgA glomerulonephritis | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:2747 | glycogen storage disease | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:1612 | breast cancer | HGNC:5012 | Homo sapiens (human) | 3161 | HMMR |
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| DOID:1205 | allergic disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:1070 | primary open angle glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:399 | tuberculosis | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:3312 | bipolar disorder | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:12449 | aplastic anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:3526 | cerebral infarction | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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| DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0060575 | 3MC syndrome 1 | HGNC:6901 | Homo sapiens (human) | 5648 | MASP1 |
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| DOID:8618 | oral cavity cancer | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:9256 | colorectal cancer | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:1612 | breast cancer | HGNC:9376 | Homo sapiens (human) | 5562 | PRKAA1 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:2018 | hyperinsulinism | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:9252 | amino acid metabolic disorder | HGNC:5005 | Homo sapiens (human) | 3155 | HMGCL |
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| DOID:2216 | factor V deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:0050453 | lissencephaly | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0110658 | congenital myasthenic syndrome 15 | HGNC:28287 | Homo sapiens (human) | 199857 | ALG14 |
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