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GlyTouCan
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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1596 | depressive disorder | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:0112383 | KINSSHIP syndrome | HGNC:6473 | Homo sapiens (human) | 3899 | AFF3 |
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| DOID:0060162 | dentatorubral-pallidoluysian atrophy | HGNC:3033 | Homo sapiens (human) | 1822 | ATN1 |
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| DOID:14778 | blepharophimosis, ptosis, and epicanthus inversus syndrome | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
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| DOID:0111140 | IGSF1 deficiency syndrome | HGNC:5948 | Homo sapiens (human) | 3547 | IGSF1 |
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| DOID:2229 | factor XI deficiency | HGNC:3529 | Homo sapiens (human) | 2160 | F11 |
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| DOID:3393 | coronary artery disease | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0110349 | osteogenesis imperfecta type 9 | HGNC:9255 | Homo sapiens (human) | 5479 | PPIB |
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| DOID:0070293 | primary autosomal recessive microcephaly 2 with or without cortical malformations | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0111533 | gnathodiaphyseal dysplasia | HGNC:27337 | Homo sapiens (human) | 203859 | ANO5 |
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| DOID:10763 | hypertension | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0070243 | primary coenzyme Q10 deficiency 6 | HGNC:20233 | Homo sapiens (human) | 51004 | COQ6 |
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| DOID:0111136 | congenital generalized lipodystrophy type 2 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:0081242 | autoimmune interstitial lung, joint, and kidney disease | HGNC:2230 | Homo sapiens (human) | 1314 | COPA |
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| DOID:1059 | intellectual disability | HGNC:3091 | Homo sapiens (human) | 1859 | DYRK1A |
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| DOID:9970 | obesity | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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| DOID:0111731 | familial episodic pain syndrome 3 | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0050857 | Perrault syndrome | HGNC:17095 | Homo sapiens (human) | 23395 | LARS2 |
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| DOID:11119 | Gilles de la Tourette syndrome | HGNC:20297 | Homo sapiens (human) | 114798 | SLITRK1 |
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| DOID:0050534 | congenital stationary night blindness | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:13994 | cleidocranial dysplasia | HGNC:10472 | Homo sapiens (human) | 860 | RUNX2 |
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| DOID:0110156 | Charcot-Marie-Tooth disease type 2B1 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:17109 | Homo sapiens (human) | 170691 | ADAMTS17 |
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