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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
LM-GlycoRepo
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:620 | blood protein disease | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:0050678 | Blau syndrome | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10961 | Homo sapiens (human) | 28234 | SLCO1B3 |
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| DOID:0080512 | Meier-Gorlin syndrome 1 | HGNC:8487 | Homo sapiens (human) | 4998 | ORC1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080735 | Ehlers-Danlos syndrome kyphoscoliotic type 2 | HGNC:18625 | Homo sapiens (human) | 55033 | FKBP14 |
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| DOID:0050562 | West syndrome | HGNC:6930 | Homo sapiens (human) | 4158 | MC2R |
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| DOID:10763 | hypertension | HGNC:17870 | Homo sapiens (human) | 27130 | INVS |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:17575 | Homo sapiens (human) | 23013 | SPEN |
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| DOID:2394 | ovarian cancer | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:2988 | antiphospholipid syndrome | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:1612 | breast cancer | HGNC:10050 | Homo sapiens (human) | 6041 | RNASEL |
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| DOID:0050922 | gastrointestinal carcinoma | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:0081267 | graft-versus-host disease | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:8923 | skin melanoma | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:0080911 | cerebrooculofacioskeletal syndrome 1 | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:1787 | pericarditis | HGNC:9364 | Homo sapiens (human) | 10216 | PRG4 |
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| DOID:3526 | cerebral infarction | HGNC:9456 | Homo sapiens (human) | 5627 | PROS1 |
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| DOID:11832 | visual epilepsy | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:4247 | coronary restenosis | HGNC:6155 | Homo sapiens (human) | 3689 | ITGB2 |
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| DOID:3753 | Hermansky-Pudlak syndrome | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
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| DOID:14723 | beta-ketothiolase deficiency | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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