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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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Repository for lectin-assisted multimodality data
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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:1324 | lung cancer | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:0110206 | Charcot-Marie-Tooth disease dominant intermediate F | HGNC:20731 | Homo sapiens (human) | 59345 | GNB4 |
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| DOID:0111995 | immunodeficiency 28 | HGNC:5440 | Homo sapiens (human) | 3460 | IFNGR2 |
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| DOID:0112315 | brain small vessel disease 3 | HGNC:26182 | Homo sapiens (human) | 79709 | COLGALT1 |
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| DOID:0080862 | primary ovarian insufficiency 5 | HGNC:22448 | Homo sapiens (human) | 135935 | NOBOX |
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| DOID:0080230 | autosomal dominant intellectual developmental disorder 54 | HGNC:1461 | Homo sapiens (human) | 816 | CAMK2B |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:0080238 | autosomal dominant intellectual developmental disorder 47 | HGNC:11354 | Homo sapiens (human) | 10274 | STAG1 |
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| DOID:0070304 | multiple epiphyseal dysplasia 3 | HGNC:2219 | Homo sapiens (human) | 1299 | COL9A3 |
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| DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
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| DOID:0111535 | progressive osseous heteroplasia | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0111377 | fetal akinesia deformation sequence syndrome 1 | HGNC:7525 | Homo sapiens (human) | 4593 | MUSK |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:0080438 | developmental and epileptic encephalopathy 5 | HGNC:11273 | Homo sapiens (human) | 6709 | SPTAN1 |
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| DOID:0112007 | growth hormone secreting pituitary adenoma 2 | HGNC:14963 | Homo sapiens (human) | 83550 | GPR101 |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0110117 | autoimmune lymphoproliferative syndrome type 4 | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:0050947 | hereditary hypophosphatemic rickets with hypercalciuria | HGNC:20305 | Homo sapiens (human) | 142680 | SLC34A3 |
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| DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:769 | neuroblastoma | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:0070124 | congenital nongoitrous hypothyroidism 2 | HGNC:8622 | Homo sapiens (human) | 7849 | PAX8 |
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| DOID:0111836 | congenital nongoitrous hypothyroidism 7 | HGNC:12299 | Homo sapiens (human) | 7201 | TRHR |
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| DOID:0050685 | small cell carcinoma | HGNC:9884 | Homo sapiens (human) | 5925 | RB1 |
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