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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:0111162 | epidermal nevus | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:2747 | glycogen storage disease | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:2394 | ovarian cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:15754 | Homo sapiens (human) | 10398 | MYL9 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:30000 | Homo sapiens (human) | 27241 | BBS9 |
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| DOID:4441 | dysgerminoma | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:10123 | pigmentation disease | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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| DOID:0001816 | angiosarcoma | HGNC:9665 | Homo sapiens (human) | 5787 | PTPRB |
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| DOID:9008 | psoriatic arthritis | HGNC:6112 | Homo sapiens (human) | 3654 | IRAK1 |
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| DOID:1148 | polydactyly | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:707 | B-cell lymphoma | HGNC:74 | Homo sapiens (human) | 9429 | ABCG2 |
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| DOID:10939 | antisocial personality disorder | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111056 | platelet-type bleeding disorder 3 | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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| DOID:0070051 | autosomal dominant intellectual developmental disorder 21 | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0050742 | nicotine dependence | HGNC:1963 | Homo sapiens (human) | 1142 | CHRNB3 |
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| DOID:0111433 | optic atrophy 3 | HGNC:8142 | Homo sapiens (human) | 80207 | OPA3 |
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| DOID:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:4029 | gastritis | HGNC:704 | Homo sapiens (human) | 10095 | ARPC1B |
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| DOID:10283 | prostate cancer | HGNC:5980 | Homo sapiens (human) | 3603 | IL16 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:16639 | Homo sapiens (human) | 23524 | SRRM2 |
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