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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:9352 | type 2 diabetes mellitus | HGNC:4192 | Homo sapiens (human) | 2642 | GCGR |
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| DOID:2942 | bronchiolitis | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:10907 | microcephaly | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:1682 | congenital heart disease | HGNC:11701 | Homo sapiens (human) | 6997 | CRIPTO |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0112337 | spermatogenic failure 55 | HGNC:26620 | Homo sapiens (human) | 200162 | SPAG17 |
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| DOID:3565 | meningioma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:2030 | anxiety disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:0080443 | developmental and epileptic encephalopathy 21 | HGNC:24539 | Homo sapiens (human) | 25977 | NECAP1 |
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| DOID:10652 | Alzheimer's disease | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:14283 | primary hypertrophic osteoarthropathy | HGNC:10955 | Homo sapiens (human) | 6578 | SLCO2A1 |
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| DOID:12206 | dengue hemorrhagic fever | HGNC:18363 | Homo sapiens (human) | 282618 | IFNL1 |
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| DOID:0111564 | hypoplastic or aplastic tibia with polydactyly | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
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| DOID:0111305 | familial febrile seizures 4 | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:1827 | idiopathic generalized epilepsy | HGNC:16882 | Homo sapiens (human) | 10021 | HCN4 |
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| DOID:9974 | drug dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:655 | inherited metabolic disorder | HGNC:10969 | Homo sapiens (human) | 6584 | SLC22A5 |
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| DOID:1307 | dementia | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:11476 | osteoporosis | HGNC:8001 | Homo sapiens (human) | 8204 | NRIP1 |
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| DOID:3070 | high grade glioma | HGNC:3437 | Homo sapiens (human) | 2073 | ERCC5 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:684 | hepatocellular carcinoma | HGNC:6973 | Homo sapiens (human) | 4193 | MDM2 |
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| DOID:0080016 | spina bifida | HGNC:7432 | Homo sapiens (human) | 4522 | MTHFD1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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