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GlyTouCan
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:10763 | hypertension | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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| DOID:0112050 | non-syndromic X-linked intellectual disability 63 | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:1059 | intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:1324 | lung cancer | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:1612 | breast cancer | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:0112050 | non-syndromic X-linked intellectual disability 63 | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:10283 | prostate cancer | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:2841 | asthma | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:9970 | obesity | HGNC:3569 | Homo sapiens (human) | 2180 | ACSL1 |
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| DOID:10283 | prostate cancer | HGNC:3560 | Homo sapiens (human) | 2171 | FABP5 |
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| DOID:8893 | psoriasis | HGNC:3560 | Homo sapiens (human) | 2171 | FABP5 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3518 | Homo sapiens (human) | 2137 | EXTL3 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3515 | Homo sapiens (human) | 2134 | EXTL1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3513 | Homo sapiens (human) | 2132 | EXT2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:3371 | chondrosarcoma | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:891 | progressive myoclonus epilepsy | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:3534 | Lafora disease | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:2977 | primary hyperoxaluria | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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