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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:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0080665 | warfarin resistance | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:9119 | acute myeloid leukemia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
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| DOID:1612 | breast cancer | HGNC:2873 | Homo sapiens (human) | 1727 | CYB5R3 |
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| DOID:12361 | Graves' disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:2237 | hepatitis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:0110196 | Charcot-Marie-Tooth disease type 4G | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:4247 | coronary restenosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050700 | cardiomyopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:7147 | ankylosing spondylitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12306 | vitiligo | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
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| DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
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| DOID:2871 | endometrial carcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0070004 | myeloid neoplasm | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:114 | heart disease | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:2957 | pulmonary tuberculosis | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:13241 | Behcet's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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