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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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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:3908 | lung non-small cell carcinoma | HGNC:9177 | Homo sapiens (human) | 5426 | POLE |
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| DOID:684 | hepatocellular carcinoma | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:3910 | lung adenocarcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:3407 | carotid artery disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:9296 | cleft lip | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:9261 | nasopharynx carcinoma | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | HGNC:430 | Homo sapiens (human) | 242 | ALOX12B |
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| DOID:399 | tuberculosis | HGNC:6338 | Homo sapiens (human) | 3811 | KIR3DL1 |
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| DOID:0111944 | immunodeficiency 31B | HGNC:11362 | Homo sapiens (human) | 6772 | STAT1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:564 | Homo sapiens (human) | 1173 | AP2M1 |
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| DOID:10605 | short bowel syndrome | HGNC:24039 | Homo sapiens (human) | 79827 | CLMP |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:0080260 | autosomal recessive spinocerebellar ataxia 26 | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:23631 | Homo sapiens (human) | 387129 | NPSR1 |
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| DOID:13241 | Behcet's disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:0111537 | paroxysmal extreme pain disorder | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:3393 | coronary artery disease | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:446 | primary hyperaldosteronism | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:1793 | pancreatic cancer | HGNC:6136 | Homo sapiens (human) | 22801 | ITGA11 |
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| DOID:0111495 | combined oxidative phosphorylation deficiency 33 | HGNC:1243 | Homo sapiens (human) | 708 | C1QBP |
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| DOID:1612 | breast cancer | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:13550 | angle-closure glaucoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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