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GlyTouCan
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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:219 | colon cancer | HGNC:7230 | Homo sapiens (human) | 4361 | MRE11 |
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| DOID:1485 | cystic fibrosis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:1967 | leiomyosarcoma | HGNC:11957 | Homo sapiens (human) | 9968 | MED12 |
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| DOID:0111530 | linear nevus sebaceous syndrome | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:591 | phobic disorder | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:10763 | hypertension | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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| DOID:0060290 | Ohdo syndrome, SBBYS variant | HGNC:17582 | Homo sapiens (human) | 23522 | KAT6B |
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| DOID:10457 | Legionnaires' disease | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:2855 | hyperthyroxinemia | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:848 | arthritis | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:0060009 | MHC class I deficiency | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:769 | neuroblastoma | HGNC:7849 | Homo sapiens (human) | 4830 | NME1 |
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| DOID:12849 | autistic disorder | HGNC:3343 | Homo sapiens (human) | 2020 | EN2 |
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| DOID:0080494 | ovarian dysgenesis 2 | HGNC:1068 | Homo sapiens (human) | 9210 | BMP15 |
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| DOID:9993 | hypoglycemia | HGNC:4335 | Homo sapiens (human) | 2746 | GLUD1 |
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| DOID:14671 | multiple intestinal atresia | HGNC:19750 | Homo sapiens (human) | 57217 | TTC7A |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:6482 | Homo sapiens (human) | 3908 | LAMA2 |
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| DOID:2044 | drug-induced hepatitis | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:2394 | ovarian cancer | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0111421 | familial apolipoprotein A5 deficiency | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:3312 | bipolar disorder | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:1407 | anterior uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2999 | granulosa cell tumor | HGNC:7059 | Homo sapiens (human) | 4255 | MGMT |
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