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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:10211 | cholelithiasis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:784 | chronic kidney disease | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:0080178 | mucositis | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:2316 | brain ischemia | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:3525 | middle cerebral artery infarction | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:2228 | thrombocytosis | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:1612 | breast cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:2841 | asthma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9970 | obesity | HGNC:9055 | Homo sapiens (human) | 5330 | PLCB2 |
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| DOID:0050546 | congenital adrenal insufficiency | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:8499 | night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:13550 | angle-closure glaucoma | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:811 | lipodystrophy | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:1826 | epilepsy | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:13366 | Stiff-Person syndrome | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:0060340 | ciliopathy | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:9351 | diabetes mellitus | HGNC:2649 | Homo sapiens (human) | 1595 | CYP51A1 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:2018 | hyperinsulinism | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:8692 | myeloid leukemia | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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