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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:2355 | anemia | HGNC:11033 | Homo sapiens (human) | 9497 | SLC4A7 |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:11033 | Homo sapiens (human) | 9497 | SLC4A7 |
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| DOID:14219 | renal tubular acidosis | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:2355 | anemia | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:10763 | hypertension | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:12387 | nephrogenic diabetes insipidus | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:4947 | cholangiocarcinoma | HGNC:11030 | Homo sapiens (human) | 8671 | SLC4A4 |
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| DOID:3159 | photosensitivity disease | HGNC:1103 | Homo sapiens (human) | 6046 | BRD2 |
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| DOID:707 | B-cell lymphoma | HGNC:1103 | Homo sapiens (human) | 6046 | BRD2 |
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| DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:1103 | Homo sapiens (human) | 6046 | BRD2 |
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| DOID:4890 | juvenile myoclonic epilepsy | HGNC:1103 | Homo sapiens (human) | 6046 | BRD2 |
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| DOID:1909 | melanoma | HGNC:1103 | Homo sapiens (human) | 6046 | BRD2 |
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| DOID:13533 | osteopetrosis | HGNC:11028 | Homo sapiens (human) | 6522 | SLC4A2 |
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| DOID:2355 | anemia | HGNC:11028 | Homo sapiens (human) | 6522 | SLC4A2 |
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| DOID:11716 | prediabetes syndrome | HGNC:11028 | Homo sapiens (human) | 6522 | SLC4A2 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:11028 | Homo sapiens (human) | 6522 | SLC4A2 |
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| DOID:11758 | iron deficiency anemia | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:2355 | anemia | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:0050700 | cardiomyopathy | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:0050758 | metabolic acidosis | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:12971 | hereditary spherocytosis | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:2373 | hereditary elliptocytosis | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:0110919 | hereditary spherocytosis type 4 | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:14219 | renal tubular acidosis | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:589 | congenital hemolytic anemia | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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