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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:3459 | breast carcinoma | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:3393 | coronary artery disease | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:11476 | osteoporosis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0050771 | pheochromocytoma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:1919 | Lesch-Nyhan syndrome | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:12365 | malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:0060602 | alpha-methylacyl-CoA racemase deficiency | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0060732 | chromosome 9p deletion syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:5199 | ureteral obstruction | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:850 | lung disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:162 | cancer | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:1184 | nephrotic syndrome | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:1883 | hepatitis C | HGNC:6374 | Homo sapiens (human) | 3821 | KLRC1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9083 | Homo sapiens (human) | 8985 | PLOD3 |
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| DOID:1596 | depressive disorder | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:10754 | otitis media | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:224 | transient cerebral ischemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:3393 | coronary artery disease | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:557 | kidney disease | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:2018 | hyperinsulinism | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:10652 | Alzheimer's disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:3310 | atopic dermatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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