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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:9352 | type 2 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:9744 | type 1 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:811 | lipodystrophy | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0111135 | congenital generalized lipodystrophy type 1 | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:5419 | schizophrenia | HGNC:703 | Homo sapiens (human) | 10552 | ARPC1A |
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| DOID:1793 | pancreatic cancer | HGNC:703 | Homo sapiens (human) | 10552 | ARPC1A |
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| DOID:13001 | carotid stenosis | HGNC:9452 | Homo sapiens (human) | 10544 | PROCR |
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| DOID:12365 | malaria | HGNC:9452 | Homo sapiens (human) | 10544 | PROCR |
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| DOID:3021 | acute kidney failure | HGNC:9452 | Homo sapiens (human) | 10544 | PROCR |
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| DOID:1508 | candidiasis | HGNC:16677 | Homo sapiens (human) | 10541 | ANP32B |
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| DOID:11476 | osteoporosis | MGI:1917329 | Mus musculus (house mouse) | 105348 | Golm1 |
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| DOID:10283 | prostate cancer | MGI:1917329 | Mus musculus (house mouse) | 105348 | Golm1 |
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| DOID:2237 | hepatitis | MGI:1917329 | Mus musculus (house mouse) | 105348 | Golm1 |
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| DOID:5082 | liver cirrhosis | MGI:1917329 | Mus musculus (house mouse) | 105348 | Golm1 |
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| DOID:684 | hepatocellular carcinoma | MGI:1917329 | Mus musculus (house mouse) | 105348 | Golm1 |
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| DOID:0050951 | hereditary ataxia | HGNC:17663 | Homo sapiens (human) | 10531 | PITRM1 |
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| DOID:0070411 | autosomal recessive spinocerebellar ataxia 30 | HGNC:17663 | Homo sapiens (human) | 10531 | PITRM1 |
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| DOID:10652 | Alzheimer's disease | HGNC:17663 | Homo sapiens (human) | 10531 | PITRM1 |
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