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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
LM-GlycoRepo
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:1793 | pancreatic cancer | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:17382 | Homo sapiens (human) | 57522 | SRGAP1 |
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| DOID:0060912 | craniosynostosis 7 | HGNC:6772 | Homo sapiens (human) | 4091 | SMAD6 |
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| DOID:0112150 | X-linked spondyloepimetaphyseal dysplasia | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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| DOID:1612 | breast cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:12894 | Sjogren's syndrome | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:14447 | gonadal dysgenesis | HGNC:1552 | Homo sapiens (human) | 84733 | CBX2 |
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| DOID:8923 | skin melanoma | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:3429 | inclusion body myositis | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0060643 | primary sclerosing cholangitis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:0111162 | epidermal nevus | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:0110674 | congenital myasthenic syndrome 17 | HGNC:6696 | Homo sapiens (human) | 4038 | LRP4 |
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| DOID:2871 | endometrial carcinoma | HGNC:10473 | Homo sapiens (human) | 864 | RUNX3 |
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| DOID:4079 | heart valve disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2018 | hyperinsulinism | HGNC:4335 | Homo sapiens (human) | 2746 | GLUD1 |
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| DOID:0070374 | leukoencephalopathy with vanishing white matter 1 | HGNC:3257 | Homo sapiens (human) | 1967 | EIF2B1 |
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| DOID:5419 | schizophrenia | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:9649 | congenital nystagmus | HGNC:10249 | Homo sapiens (human) | 6091 | ROBO1 |
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| DOID:10223 | dermatomyositis | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:576 | proteinuria | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:399 | tuberculosis | HGNC:7997 | Homo sapiens (human) | 3084 | NRG1 |
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| DOID:783 | end stage renal disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:15879 | Homo sapiens (human) | 56259 | CTNNBL1 |
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