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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:1380 | endometrial cancer | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:3459 | breast carcinoma | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:0081292 | traumatic brain injury | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:4676 | uremia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:10763 | hypertension | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:11054 | urinary bladder cancer | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:13129 | severe pre-eclampsia | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:3770 | pulmonary fibrosis | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:0080322 | polycystic kidney disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:3068 | glioblastoma | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:3393 | coronary artery disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:10629 | microphthalmia | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:2237 | hepatitis | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:9675 | pulmonary emphysema | HGNC:4019 | Homo sapiens (human) | 2530 | FUT8 |
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| DOID:2723 | dermatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11054 | urinary bladder cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0110721 | neuronal ceroid lipofuscinosis 1 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:206 | hereditary multiple exostoses | HGNC:3518 | Homo sapiens (human) | 2137 | EXTL3 |
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| DOID:2799 | bronchiolitis obliterans | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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