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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:9352 | type 2 diabetes mellitus | HGNC:12711 | Homo sapiens (human) | 9559 | VPS26A |
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| DOID:1930 | Laurence-Moon syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:6819 | Homo sapiens (human) | 10892 | MALT1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:12020 | Homo sapiens (human) | 8460 | TPST1 |
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| DOID:0111785 | frontometaphyseal dysplasia | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:5844 | myocardial infarction | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:0060475 | myoclonic-atonic epilepsy | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:1470 | major depressive disorder | HGNC:11957 | Homo sapiens (human) | 9968 | MED12 |
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| DOID:0050774 | rapadilino syndrome | HGNC:9949 | Homo sapiens (human) | 9401 | RECQL4 |
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| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0060286 | combined oxidative phosphorylation deficiency | HGNC:26223 | Homo sapiens (human) | 79736 | TEFM |
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| DOID:1936 | atherosclerosis | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:0050598 | extrapulmonary tuberculosis | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:2773 | contact dermatitis | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0080315 | megalencephalic leukoencephalopathy with subcortical cysts | HGNC:13308 | Homo sapiens (human) | 51704 | GPRC5B |
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| DOID:9970 | obesity | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:127 | leiomyoma | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:0112300 | spondylometaphyseal dysplasia with cone-rod dystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0081225 | autosomal recessive intellectual developmental disorder 64 | HGNC:21205 | Homo sapiens (human) | 84894 | LINGO1 |
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| DOID:3407 | carotid artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:7148 | rheumatoid arthritis | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:8866 | actinic keratosis | HGNC:8101 | Homo sapiens (human) | 4948 | OCA2 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:12559 | idiopathic juvenile osteoporosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
|
