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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:0110916 | hereditary spherocytosis type 1 | HGNC:244 | Homo sapiens (human) | 119 | ADD2 |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | HGNC:244 | Homo sapiens (human) | 119 | ADD2 |
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| DOID:5419 | schizophrenia | MGI:1098567 | Mus musculus (house mouse) | 11899 | Astn1 |
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| DOID:0050888 | syndromic intellectual disability | HGNC:26974 | Homo sapiens (human) | 118987 | PDZD8 |
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| DOID:684 | hepatocellular carcinoma | MGI:88090 | Mus musculus (house mouse) | 11898 | Ass1 |
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| DOID:13141 | uveitis | MGI:88090 | Mus musculus (house mouse) | 11898 | Ass1 |
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| DOID:1909 | melanoma | MGI:88090 | Mus musculus (house mouse) | 11898 | Ass1 |
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| DOID:0070340 | classic citrullinemia | MGI:88090 | Mus musculus (house mouse) | 11898 | Ass1 |
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| DOID:10652 | Alzheimer's disease | MGI:88090 | Mus musculus (house mouse) | 11898 | Ass1 |
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| DOID:9273 | citrullinemia | MGI:88090 | Mus musculus (house mouse) | 11898 | Ass1 |
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| DOID:1927 | sphingolipidosis | MGI:1277124 | Mus musculus (house mouse) | 11886 | Asah1 |
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| DOID:0050464 | Farber lipogranulomatosis | MGI:1277124 | Mus musculus (house mouse) | 11886 | Asah1 |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | MGI:1277124 | Mus musculus (house mouse) | 11886 | Asah1 |
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| DOID:0050545 | visceral heterotaxy | HGNC:14357 | Homo sapiens (human) | 118856 | MMP21 |
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| DOID:1459 | hypothyroidism | MGI:88077 | Mus musculus (house mouse) | 11883 | Arsa |
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| DOID:10581 | metachromatic leukodystrophy | MGI:88077 | Mus musculus (house mouse) | 11883 | Arsa |
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| DOID:12800 | mucopolysaccharidosis VI | MGI:88075 | Mus musculus (house mouse) | 11881 | Arsb |
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| DOID:0110146 | Bartter disease type 4b | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:12387 | nephrogenic diabetes insipidus | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:445 | Bartter disease | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:423 | myopathy | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:0110144 | Bartter disease type 3 | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:0050450 | Gitelman syndrome | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:10763 | hypertension | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:1793 | pancreatic cancer | MGI:1333791 | Mus musculus (house mouse) | 11876 | Artn |
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