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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:11832 | visual epilepsy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9743 | diabetic neuropathy | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:3526 | cerebral infarction | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:4231 | histiocytoma | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:5199 | ureteral obstruction | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12306 | vitiligo | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0060050 | autoimmune disease of blood | HGNC:24337 | Homo sapiens (human) | 56913 | C1GALT1 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5008 | Homo sapiens (human) | 3158 | HMGCS2 |
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| DOID:11476 | osteoporosis | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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| DOID:552 | pneumonia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9452 | steatotic liver disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0060575 | 3MC syndrome 1 | HGNC:6901 | Homo sapiens (human) | 5648 | MASP1 |
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| DOID:0080197 | congenital muscular dystrophy with cataracts and intellectual disability | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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| DOID:104 | bacterial infectious disease | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:8618 | oral cavity cancer | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:9256 | colorectal cancer | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:13452 | scleritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1612 | breast cancer | HGNC:9376 | Homo sapiens (human) | 5562 | PRKAA1 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0090001 | Fraser syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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