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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:3883 | Lynch syndrome | HGNC:16261 | Homo sapiens (human) | 114571 | SLC22A9 |
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| DOID:999 | hypereosinophilic syndrome | HGNC:8803 | Homo sapiens (human) | 5156 | PDGFRA |
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| DOID:5426 | primary ovarian insufficiency | HGNC:7327 | Homo sapiens (human) | 4438 | MSH4 |
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| DOID:114 | heart disease | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:0060572 | Ritscher-Schinzel syndrome 2 | HGNC:28909 | Homo sapiens (human) | 28952 | CCDC22 |
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| DOID:4247 | coronary restenosis | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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| DOID:0112018 | non-syndromic X-linked intellectual disability 104 | HGNC:29007 | Homo sapiens (human) | 9758 | FRMPD4 |
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| DOID:104 | bacterial infectious disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0112249 | GAPO syndrome | HGNC:21014 | Homo sapiens (human) | 84168 | ANTXR1 |
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| DOID:11832 | visual epilepsy | RGD:2949 | Rattus norvegicus (Norway rat) | 24520 | Kcna1 |
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| DOID:0111258 | pentosuria | HGNC:18985 | Homo sapiens (human) | 51181 | DCXR |
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| DOID:1749 | squamous cell carcinoma | HGNC:13726 | Homo sapiens (human) | 58508 | KMT2C |
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| DOID:11476 | osteoporosis | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0111844 | X-linked intellectual developmental disorder 108 | HGNC:17123 | Homo sapiens (human) | 84679 | SLC9A7 |
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| DOID:0112243 | congenital symmetric circumferential skin creases 2 | HGNC:6891 | Homo sapiens (human) | 10982 | MAPRE2 |
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| DOID:4051 | alveolar rhabdomyosarcoma | HGNC:3819 | Homo sapiens (human) | 2308 | FOXO1 |
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| DOID:1909 | melanoma | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:12859 | choreatic disease | HGNC:1908 | Homo sapiens (human) | 23230 | VPS13A |
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| DOID:2222 | factor X deficiency | HGNC:3528 | Homo sapiens (human) | 2159 | F10 |
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| DOID:0081224 | autosomal recessive intellectual developmental disorder 63 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:9884 | muscular dystrophy | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:1612 | breast cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0112348 | hereditary spastic paraplegia 78 | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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| DOID:0080632 | Fazio-Londe disease | HGNC:16187 | Homo sapiens (human) | 113278 | SLC52A3 |
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| DOID:0111286 | psoriasis 1 | HGNC:4933 | Homo sapiens (human) | 3107 | HLA-C |
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