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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:9744 | type 1 diabetes mellitus | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:5419 | schizophrenia | HGNC:5295 | Homo sapiens (human) | 3358 | HTR2C |
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| DOID:3347 | osteosarcoma | HGNC:1743 | Homo sapiens (human) | 988 | CDC5L |
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| DOID:10652 | Alzheimer's disease | HGNC:11741 | Homo sapiens (human) | 7019 | TFAM |
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| DOID:12930 | dilated cardiomyopathy | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0111623 | ACTH-independent macronodular adrenal hyperplasia 1 | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | HGNC:1152 | Homo sapiens (human) | 11149 | BVES |
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| DOID:14766 | renal agenesis | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:1349 | Homo sapiens (human) | 219285 | SAMD9L |
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| DOID:0080954 | arthrogryposis multiplex congenita | HGNC:17089 | Homo sapiens (human) | 23345 | SYNE1 |
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| DOID:11054 | urinary bladder cancer | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:5844 | myocardial infarction | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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| DOID:0080135 | multiple mitochondrial dysfunctions syndrome 3 | HGNC:27302 | Homo sapiens (human) | 200205 | IBA57 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:13001 | carotid stenosis | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:0060817 | syndromic X-linked intellectual disability 34 | HGNC:7871 | Homo sapiens (human) | 4841 | NONO |
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| DOID:0111955 | immunodeficiency 27A | HGNC:5439 | Homo sapiens (human) | 3459 | IFNGR1 |
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| DOID:5082 | liver cirrhosis | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:11054 | urinary bladder cancer | HGNC:10473 | Homo sapiens (human) | 864 | RUNX3 |
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| DOID:4586 | familial meningioma | HGNC:7180 | Homo sapiens (human) | 4330 | MN1 |
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| DOID:5844 | myocardial infarction | HGNC:6701 | Homo sapiens (human) | 4043 | LRPAP1 |
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| DOID:0050784 | primary progressive multiple sclerosis | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:12176 | goiter | HGNC:11764 | Homo sapiens (human) | 7038 | TG |
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| DOID:0111228 | Sveinsson chorioretinal atrophy | HGNC:11714 | Homo sapiens (human) | 7003 | TEAD1 |
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