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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050771 | pheochromocytoma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:23019 | Homo sapiens (human) | 8233 | ZRSR2 |
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| DOID:1612 | breast cancer | HGNC:5960 | Homo sapiens (human) | 3551 | IKBKB |
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| DOID:0112346 | hereditary spastic paraplegia 83 | HGNC:28242 | Homo sapiens (human) | 84842 | HPDL |
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| DOID:1324 | lung cancer | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0080686 | tubular aggregate myopathy 2 | HGNC:25896 | Homo sapiens (human) | 84876 | ORAI1 |
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| DOID:0080569 | congenital disorder of glycosylation Ir | HGNC:2728 | Homo sapiens (human) | 1650 | DDOST |
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| DOID:988 | mitral valve prolapse | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:10652 | Alzheimer's disease | HGNC:6701 | Homo sapiens (human) | 4043 | LRPAP1 |
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| DOID:0111079 | birdshot chorioretinopathy | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:2729 | dyskeratosis congenita | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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| DOID:2602 | chondroma | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
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| DOID:1825 | childhood absence epilepsy | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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| DOID:3070 | high grade glioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:10939 | antisocial personality disorder | HGNC:5287 | Homo sapiens (human) | 3351 | HTR1B |
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| DOID:1798 | pancreatic endocrine carcinoma | HGNC:2681 | Homo sapiens (human) | 1616 | DAXX |
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| DOID:612 | primary immunodeficiency disease | HGNC:29418 | Homo sapiens (human) | 96459 | FNIP1 |
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| DOID:0080086 | nonsyndromic congenital nail disorder 8 | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0112334 | pontocerebellar hypoplasia type 1C | HGNC:17035 | Homo sapiens (human) | 11340 | EXOSC8 |
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| DOID:9351 | diabetes mellitus | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0050864 | non-arteritic anterior ischemic optic neuropathy | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:8778 | Crohn's disease | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:2723 | dermatitis | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:3209 | junctional epidermolysis bullosa | HGNC:6158 | Homo sapiens (human) | 3691 | ITGB4 |
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| DOID:1793 | pancreatic cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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