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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:612 | primary immunodeficiency disease | HGNC:17967 | Homo sapiens (human) | 51135 | IRAK4 |
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| DOID:0111376 | fetal akinesia deformation sequence syndrome 3 | HGNC:26594 | Homo sapiens (human) | 285489 | DOK7 |
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| DOID:0111686 | hereditary mixed polyposis syndrome 2 | HGNC:1076 | Homo sapiens (human) | 657 | BMPR1A |
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| DOID:0080468 | developmental and epileptic encephalopathy 1 | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0111380 | solitary median maxillary central incisor | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0090078 | hypogonadotropic hypogonadism 7 with or without anosmia | HGNC:29843 | Homo sapiens (human) | 26012 | NSMF |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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| DOID:0110247 | cataract 36 | HGNC:30831 | Homo sapiens (human) | 23424 | TDRD7 |
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| DOID:3307 | teratoma | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:7148 | rheumatoid arthritis | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:4448 | macular degeneration | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:1612 | breast cancer | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:12678 | hypercalcemia | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:10283 | prostate cancer | HGNC:4910 | Homo sapiens (human) | 3091 | HIF1A |
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| DOID:11335 | sarcoidosis | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:0111984 | immunodeficiency 58 | HGNC:27089 | Homo sapiens (human) | 146206 | CARMIL2 |
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| DOID:0070140 | autosomal recessive cutis laxa type IIC | HGNC:857 | Homo sapiens (human) | 529 | ATP6V1E1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:603 | Homo sapiens (human) | 338 | APOB |
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| DOID:0111462 | cardiofaciocutaneous syndrome 3 | HGNC:6840 | Homo sapiens (human) | 5604 | MAP2K1 |
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| DOID:1205 | allergic disease | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:3393 | coronary artery disease | HGNC:2024 | Homo sapiens (human) | 1185 | CLCN6 |
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| DOID:9663 | aphthous stomatitis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:9477 | pulmonary embolism | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:0111536 | Buschke-Ollendorff syndrome | HGNC:28887 | Homo sapiens (human) | 23592 | LEMD3 |
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