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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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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:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:9970 | obesity | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:13372 | alpha 1-antitrypsin deficiency | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:0050816 | urofacial syndrome | HGNC:18374 | Homo sapiens (human) | 60495 | HPSE2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18431 | Homo sapiens (human) | 10965 | ACOT2 |
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| DOID:9970 | obesity | HGNC:18448 | Homo sapiens (human) | 79661 | NEIL1 |
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| DOID:0060611 | abdominal obesity-metabolic syndrome | HGNC:18448 | Homo sapiens (human) | 79661 | NEIL1 |
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| DOID:224 | transient cerebral ischemia | HGNC:18451 | Homo sapiens (human) | 90411 | MCFD2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:3153 | lipomatosis | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:14219 | renal tubular acidosis | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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