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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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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:0050934 | ovarian clear cell carcinoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0070042 | Coffin-Siris syndrome 1 | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:6713 | cerebrovascular disease | HGNC:15607 | Homo sapiens (human) | 8874 | ARHGEF7 |
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| DOID:1059 | intellectual disability | HGNC:685 | Homo sapiens (human) | 9459 | ARHGEF6 |
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| DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | HGNC:682 | Homo sapiens (human) | 9181 | ARHGEF2 |
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| DOID:10941 | intracranial aneurysm | HGNC:21726 | Homo sapiens (human) | 9828 | ARHGEF17 |
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| DOID:2843 | long QT syndrome | HGNC:26388 | Homo sapiens (human) | 158763 | ARHGAP36 |
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| DOID:0060041 | autism spectrum disorder | HGNC:17399 | Homo sapiens (human) | 9743 | ARHGAP32 |
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| DOID:3393 | coronary artery disease | HGNC:29216 | Homo sapiens (human) | 57514 | ARHGAP31 |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:29216 | Homo sapiens (human) | 57514 | ARHGAP31 |
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| DOID:0080311 | X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance | HGNC:17073 | Homo sapiens (human) | 23092 | ARHGAP26 |
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| DOID:0081082 | acute myelomonocytic leukemia | HGNC:17073 | Homo sapiens (human) | 23092 | ARHGAP26 |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:17073 | Homo sapiens (human) | 23092 | ARHGAP26 |
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| DOID:9408 | acute myocardial infarction | HGNC:18239 | Homo sapiens (human) | 55114 | ARHGAP17 |
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| DOID:0112258 | N-acetylglutamate synthase deficiency | SGD:S000003607 | Saccharomyces cerevisiae S288C | 853374 | ARG2 |
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| DOID:9252 | amino acid metabolic disorder | SGD:S000003607 | Saccharomyces cerevisiae S288C | 853374 | ARG2 |
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| DOID:0050454 | periventricular nodular heterotopia | HGNC:15853 | Homo sapiens (human) | 10564 | ARFGEF2 |
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| DOID:8634 | prostate carcinoma in situ | HGNC:651 | Homo sapiens (human) | 374 | AREG |
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| DOID:3070 | high grade glioma | HGNC:651 | Homo sapiens (human) | 374 | AREG |
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| DOID:11054 | urinary bladder cancer | HGNC:651 | Homo sapiens (human) | 374 | AREG |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:651 | Homo sapiens (human) | 374 | AREG |
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| DOID:3008 | invasive ductal carcinoma | HGNC:651 | Homo sapiens (human) | 374 | AREG |
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| DOID:2671 | transitional cell carcinoma | HGNC:651 | Homo sapiens (human) | 374 | AREG |
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| DOID:1612 | breast cancer | HGNC:651 | Homo sapiens (human) | 374 | AREG |
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