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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:5844 | myocardial infarction | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:5844 | myocardial infarction | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:10825 | essential hypertension | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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| DOID:4483 | rhinitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0070459 | hereditary spastic paraplegia 90A | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:1612 | breast cancer | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:8029 | sporadic breast cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:161 | keratosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:8505 | dermatitis herpetiformis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5742 | pancreatic acinar cell adenocarcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:10534 | stomach cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0090103 | Huntington's disease-like 1 | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8973 | Homo sapiens (human) | 5288 | PIK3C2G |
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| DOID:9970 | obesity | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:0111223 | centronuclear myopathy 1 | HGNC:26190 | Homo sapiens (human) | 64419 | MTMR14 |
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| DOID:0050697 | chorioamnionitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10763 | hypertension | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:3526 | cerebral infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | HGNC:23213 | Homo sapiens (human) | 284098 | PIGW |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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