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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
LM-GlycoRepo
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:2671 | transitional cell carcinoma | HGNC:1116 | Homo sapiens (human) | 682 | BSG |
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| DOID:4450 | renal cell carcinoma | HGNC:1116 | Homo sapiens (human) | 682 | BSG |
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| DOID:0050585 | congenital generalized lipodystrophy | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:12336 | male infertility | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:14227 | azoospermia | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:811 | lipodystrophy | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:0111136 | congenital generalized lipodystrophy type 2 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:0110770 | hereditary spastic paraplegia 17 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:0081401 | autosomal dominant distal hereditary motor neuronopathy 13 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:0112045 | non-syndromic X-linked intellectual disability 93 | HGNC:17342 | Homo sapiens (human) | 254065 | BRWD3 |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:12760 | Homo sapiens (human) | 54014 | BRWD1 |
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| DOID:0050888 | syndromic intellectual disability | HGNC:14255 | Homo sapiens (human) | 7862 | BRPF1 |
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| DOID:3393 | coronary artery disease | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:1474 | aggressive periodontitis | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:0050865 | tongue squamous cell carcinoma | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:8577 | ulcerative colitis | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:3388 | periodontal disease | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:5844 | myocardial infarction | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:3526 | cerebral infarction | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:13746 | Homo sapiens (human) | 57795 | BRINP2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:2687 | Homo sapiens (human) | 1620 | BRINP1 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:2687 | Homo sapiens (human) | 1620 | BRINP1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:19874 | Homo sapiens (human) | 10902 | BRD8 |
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| DOID:3069 | malignant astrocytoma | HGNC:14310 | Homo sapiens (human) | 29117 | BRD7 |
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