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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:6432 | pulmonary hypertension | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:2977 | primary hyperoxaluria | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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| DOID:1891 | optic nerve disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:4621 | holoprosencephaly | HGNC:29185 | Homo sapiens (human) | 23007 | PLCH1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12858 | Huntington's disease | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:6457 | Cowden syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:13482 | Proteus syndrome | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:5844 | myocardial infarction | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:10603 | glucose intolerance | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:9970 | obesity | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:9675 | pulmonary emphysema | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:10763 | hypertension | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:11396 | pulmonary edema | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:552 | pneumonia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1682 | congenital heart disease | HGNC:12757 | Homo sapiens (human) | 11091 | WDR5 |
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| DOID:13375 | temporal arteritis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:3407 | carotid artery disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:14330 | Parkinson's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:5419 | schizophrenia | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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