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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:4450 | renal cell carcinoma | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:1612 | breast cancer | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:10283 | prostate cancer | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:10763 | hypertension | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:8778 | Crohn's disease | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:8577 | ulcerative colitis | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:3312 | bipolar disorder | SGD:S000005163 | Saccharomyces cerevisiae S288C | 855502 | ALG9 |
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| DOID:0080564 | congenital disorder of glycosylation Il | SGD:S000005163 | Saccharomyces cerevisiae S288C | 855502 | ALG9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005163 | Saccharomyces cerevisiae S288C | 855502 | ALG9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:0080560 | congenital disorder of glycosylation Ih | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0050770 | polycystic liver disease | SGD:S000005593 | Saccharomyces cerevisiae S288C | 854233 | ALG8 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005593 | Saccharomyces cerevisiae S288C | 854233 | ALG8 |
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| DOID:0050770 | polycystic liver disease | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0080560 | congenital disorder of glycosylation Ih | SGD:S000005593 | Saccharomyces cerevisiae S288C | 854233 | ALG8 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | SGD:S000000447 | Saccharomyces cerevisiae S288C | 852545 | ALG7 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | SGD:S000000447 | Saccharomyces cerevisiae S288C | 852545 | ALG7 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005528 | Saccharomyces cerevisiae S288C | 854163 | ALG6 |
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| DOID:0080555 | congenital disorder of glycosylation Ic | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0080555 | congenital disorder of glycosylation Ic | SGD:S000005528 | Saccharomyces cerevisiae S288C | 854163 | ALG6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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