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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:783 | end stage renal disease | HGNC:6357 | Homo sapiens (human) | 3816 | KLK1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:12177 | common variable immunodeficiency | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:10941 | intracranial aneurysm | HGNC:3349 | Homo sapiens (human) | 2022 | ENG |
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| DOID:2841 | asthma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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| DOID:0111997 | immunodeficiency 63 | HGNC:6009 | Homo sapiens (human) | 3560 | IL2RB |
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| DOID:4751 | striatonigral degeneration | HGNC:8066 | Homo sapiens (human) | 23636 | NUP62 |
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| DOID:14213 | hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:6543 | acne | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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| DOID:0110824 | hereditary spastic paraplegia 9A | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0112358 | short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | HGNC:13655 | Homo sapiens (human) | 222663 | SCUBE3 |
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| DOID:9296 | cleft lip | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0050685 | small cell carcinoma | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:17574 | Homo sapiens (human) | 57538 | ALPK3 |
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| DOID:0081288 | white sponge nevus 2 | HGNC:6415 | Homo sapiens (human) | 3860 | KRT13 |
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| DOID:9119 | acute myeloid leukemia | HGNC:15514 | Homo sapiens (human) | 8301 | PICALM |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:11713 | diabetic angiopathy | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:6000 | congestive heart failure | HGNC:18145 | Homo sapiens (human) | 84295 | PHF6 |
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| DOID:2451 | protein S deficiency | HGNC:9456 | Homo sapiens (human) | 5627 | PROS1 |
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| DOID:9256 | colorectal cancer | HGNC:6190 | Homo sapiens (human) | 3716 | JAK1 |
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| DOID:0111341 | primary failure of tooth eruption | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:1612 | breast cancer | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:3132 | porphyria cutanea tarda | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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