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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:14504 | Niemann-Pick disease | HGNC:7897 | Homo sapiens (human) | 4864 | NPC1 |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:299 | adenocarcinoma | HGNC:6710 | Homo sapiens (human) | 4048 | LTA4H |
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| DOID:10762 | portal hypertension | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:224 | transient cerebral ischemia | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:3178 | skin papilloma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:234 | colon adenocarcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:0112300 | spondylometaphyseal dysplasia with cone-rod dystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:5679 | retinal disease | HGNC:24289 | Homo sapiens (human) | 10390 | CEPT1 |
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| DOID:9538 | multiple myeloma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:8947 | diabetic retinopathy | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:9261 | nasopharynx carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:607 | paraplegia | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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| DOID:0080005 | bone remodeling disease | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:11476 | osteoporosis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:6432 | pulmonary hypertension | HGNC:4818 | Homo sapiens (human) | 3036 | HAS1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:4450 | renal cell carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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| DOID:2580 | rhizomelic chondrodysplasia punctata | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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