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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:1733 | cryptosporidiosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:350 | mastocytosis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:0080943 | 46,XX sex reversal 5 | HGNC:7976 | Homo sapiens (human) | 7026 | NR2F2 |
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| DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:14899 | Homo sapiens (human) | 140766 | ADAMTS14 |
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| DOID:612 | primary immunodeficiency disease | HGNC:25941 | Homo sapiens (human) | 54790 | TET2 |
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| DOID:0111696 | familial adult myoclonic epilepsy 6 | HGNC:11969 | Homo sapiens (human) | 27327 | TNRC6A |
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| DOID:0110989 | Joubert syndrome 20 | HGNC:37234 | Homo sapiens (human) | 79583 | TMEM231 |
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| DOID:2355 | anemia | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:0060903 | thrombosis | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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| DOID:0081216 | autosomal recessive intellectual developmental disorder 54 | HGNC:30765 | Homo sapiens (human) | 23043 | TNIK |
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| DOID:12361 | Graves' disease | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:1612 | breast cancer | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:281 | Homo sapiens (human) | 150 | ADRA2A |
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| DOID:0081440 | Peroxisome biogenesis disorder 10B | HGNC:8858 | Homo sapiens (human) | 8504 | PEX3 |
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| DOID:0070526 | PLACK syndrome | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:9253 | Homo sapiens (human) | 5478 | PPIA |
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| DOID:9778 | irritable bowel syndrome | HGNC:5297 | Homo sapiens (human) | 3359 | HTR3A |
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| DOID:5844 | myocardial infarction | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:0080079 | nonsyndromic congenital nail disorder 1 | HGNC:4044 | Homo sapiens (human) | 8323 | FZD6 |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:0110749 | type 1 diabetes mellitus 10 | HGNC:6008 | Homo sapiens (human) | 3559 | IL2RA |
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| DOID:0110212 | Charcot-Marie-Tooth disease X-linked recessive 4 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:3565 | meningioma | HGNC:7180 | Homo sapiens (human) | 4330 | MN1 |
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| DOID:9256 | colorectal cancer | HGNC:9673 | Homo sapiens (human) | 5795 | PTPRJ |
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| DOID:0111247 | hypertension and brachydactyly syndrome | HGNC:8778 | Homo sapiens (human) | 5139 | PDE3A |
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