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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:3907 | lung squamous cell carcinoma | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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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: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:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:7575 | pancreatic intraductal papillary-mucinous neoplasm | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080568 | congenital disorder of glycosylation Iq | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:409 | liver disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10591 | pre-eclampsia | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0080176 | meningococcal meningitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:783 | end stage renal disease | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:13774 | Addison's disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:0050567 | orofacial cleft | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:10763 | hypertension | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:5844 | myocardial infarction | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0110435 | dilated cardiomyopathy 1GG | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:10003 | sensorineural hearing loss | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:13564 | aspergillosis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:9119 | acute myeloid leukemia | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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