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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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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:3312 | bipolar disorder | HGNC:17089 | Homo sapiens (human) | 23345 | SYNE1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:6371 | Homo sapiens (human) | 3818 | KLKB1 |
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| DOID:0050697 | chorioamnionitis | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:9008 | psoriatic arthritis | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:2394 | ovarian cancer | HGNC:8143 | Homo sapiens (human) | 4978 | OPCML |
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| DOID:13189 | gout | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0111945 | immunodeficiency 31A | HGNC:11362 | Homo sapiens (human) | 6772 | STAT1 |
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| DOID:3119 | gastrointestinal system cancer | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:3234 | central nervous system lymphoma | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0111902 | thrombophilia due to activated protein C resistance | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:0080234 | Clark-Baraitser syndrome | HGNC:12306 | Homo sapiens (human) | 9320 | TRIP12 |
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| DOID:12236 | primary biliary cholangitis | HGNC:45 | Homo sapiens (human) | 5244 | ABCB4 |
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| DOID:684 | hepatocellular carcinoma | RGD:621871 | Rattus norvegicus (Norway rat) | 26195 | COX1 |
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| DOID:10763 | hypertension | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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| DOID:0060781 | congenital secretory sodium diarrhea 3 | HGNC:11247 | Homo sapiens (human) | 10653 | SPINT2 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0111025 | cone-rod dystrophy 19 | HGNC:19963 | Homo sapiens (human) | 23093 | TTLL5 |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:8011 | Homo sapiens (human) | 8506 | CNTNAP1 |
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| DOID:0050328 | congenital hypothyroidism | HGNC:11040 | Homo sapiens (human) | 6528 | SLC5A5 |
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| DOID:10763 | hypertension | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:0070187 | Y-linked spermatogenic failure 2 | HGNC:12633 | Homo sapiens (human) | 8287 | USP9Y |
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| DOID:5419 | schizophrenia | HGNC:4041 | Homo sapiens (human) | 7976 | FZD3 |
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| DOID:3393 | coronary artery disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:4450 | renal cell carcinoma | HGNC:30064 | Homo sapiens (human) | 55193 | PBRM1 |
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