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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3082 | interstitial lung disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:8577 | ulcerative colitis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:1380 | endometrial cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:10283 | prostate cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:11713 | diabetic angiopathy | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:9976 | heroin dependence | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:8634 | prostate carcinoma in situ | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:9111 | cutaneous leishmaniasis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:127 | leiomyoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0060611 | abdominal obesity-metabolic syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:769 | neuroblastoma | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:4450 | renal cell carcinoma | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:2871 | endometrial carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:5723 | optic atrophy | HGNC:29622 | Homo sapiens (human) | 27349 | MCAT |
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| DOID:9884 | muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:670 | amphetamine abuse | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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