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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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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:0111809 | syndromic microphthalmia 2 | MGI:1918708 | Mus musculus (house mouse) | 71458 | Bcor |
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| DOID:10534 | stomach cancer | MGI:1918708 | Mus musculus (house mouse) | 71458 | Bcor |
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| DOID:0060249 | scoliosis | MGI:1918711 | Mus musculus (house mouse) | 71461 | Ptk7 |
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| DOID:0060250 | idiopathic scoliosis | MGI:1918711 | Mus musculus (house mouse) | 71461 | Ptk7 |
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| DOID:9620 | vesicoureteral reflux | HGNC:11976 | Homo sapiens (human) | 7148 | TNXB |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:11976 | Homo sapiens (human) | 7148 | TNXB |
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| DOID:0080986 | Ehlers-Danlos syndrome periodontal type 1 | HGNC:1246 | Homo sapiens (human) | 715 | C1R |
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| DOID:162 | cancer | HGNC:11986 | Homo sapiens (human) | 7150 | TOP1 |
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| DOID:0060565 | Ritscher-Schinzel syndrome | MGI:1918767 | Mus musculus (house mouse) | 71517 | Vps35l |
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| DOID:10283 | prostate cancer | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:2115 | B cell deficiency | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:8991 | cervix uteri carcinoma in situ | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:9119 | acute myeloid leukemia | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:162 | cancer | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:11624 | penile benign neoplasm | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:11054 | urinary bladder cancer | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:2154 | nephroblastoma | HGNC:11989 | Homo sapiens (human) | 7153 | TOP2A |
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| DOID:162 | cancer | HGNC:11990 | Homo sapiens (human) | 7155 | TOP2B |
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| DOID:9119 | acute myeloid leukemia | HGNC:11990 | Homo sapiens (human) | 7155 | TOP2B |
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| DOID:2115 | B cell deficiency | HGNC:11990 | Homo sapiens (human) | 7155 | TOP2B |
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| DOID:0111524 | autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5 | HGNC:11992 | Homo sapiens (human) | 7156 | TOP3A |
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| DOID:10605 | short bowel syndrome | MGI:1918816 | Mus musculus (house mouse) | 71566 | Clmp |
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| DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3702 | cervical adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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