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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050933 | ovarian serous carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:4897 | bile duct carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:684 | hepatocellular carcinoma | HGNC:24573 | Homo sapiens (human) | 55247 | NEIL3 |
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| DOID:0111027 | hemochromatosis type 2A | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:1612 | breast cancer | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3314 | angiomyolipoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:10283 | prostate cancer | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0080016 | spina bifida | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:9538 | multiple myeloma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:10763 | hypertension | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:1168 | familial hyperlipidemia | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:6846 | familial melanoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:7998 | hyperthyroidism | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:10587 | Krabbe disease | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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| DOID:3021 | acute kidney failure | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3454 | brain infarction | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:11801 | protein-energy malnutrition | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1287 | cardiovascular system disease | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:12930 | dilated cardiomyopathy | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:3312 | bipolar disorder | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:4450 | renal cell carcinoma | HGNC:9238 | Homo sapiens (human) | 5471 | PPAT |
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