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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:0080855 | Parkinsonism | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0112313 | brain small vessel disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:5082 | liver cirrhosis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:4676 | uremia | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:9970 | obesity | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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| DOID:83 | cataract | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:0112319 | Kanzaki disease | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:2316 | brain ischemia | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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| DOID:10652 | Alzheimer's disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:6543 | acne | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10763 | hypertension | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:1824 | status epilepticus | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:1459 | hypothyroidism | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:5082 | liver cirrhosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9970 | obesity | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:1926 | Gaucher's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:18859 | Homo sapiens (human) | 56848 | SPHK2 |
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| DOID:9538 | multiple myeloma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:8893 | psoriasis | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:11088 | asphyxia neonatorum | HGNC:4606 | Homo sapiens (human) | 2923 | PDIA3 |
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