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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
LM-GlycoRepo
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:0110454 | dilated cardiomyopathy 1S | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:0060556 | Kufor-Rakeb syndrome | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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| DOID:0050887 | Townes-Brocks syndrome | HGNC:10524 | Homo sapiens (human) | 6299 | SALL1 |
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| DOID:0110869 | congenital stationary night blindness 1E | HGNC:31371 | Homo sapiens (human) | 440435 | GPR179 |
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| DOID:0111385 | inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0060878 | hypoparathyroidism-deafness-renal disease syndrome | HGNC:4172 | Homo sapiens (human) | 2625 | GATA3 |
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| DOID:0080887 | vitamin D-dependent rickets type 1B | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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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:0111140 | IGSF1 deficiency syndrome | HGNC:5948 | Homo sapiens (human) | 3547 | IGSF1 |
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| DOID:0110349 | osteogenesis imperfecta type 9 | HGNC:9255 | Homo sapiens (human) | 5479 | PPIB |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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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: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:0050475 | Weill-Marchesani syndrome | HGNC:17109 | Homo sapiens (human) | 170691 | ADAMTS17 |
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| DOID:0110337 | osteogenesis imperfecta type 7 | HGNC:2379 | Homo sapiens (human) | 10491 | CRTAP |
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| DOID:0050545 | visceral heterotaxy | HGNC:14357 | Homo sapiens (human) | 118856 | MMP21 |
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| DOID:0070416 | Luo-Schoch-Yamamoto syndrome | HGNC:10061 | Homo sapiens (human) | 6045 | RNF2 |
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| DOID:0080212 | polycystic kidney disease 4 | HGNC:9016 | Homo sapiens (human) | 5314 | PKHD1 |
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| DOID:0080463 | developmental and epileptic encephalopathy 33 | HGNC:3192 | Homo sapiens (human) | 1917 | EEF1A2 |
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| DOID:14743 | trichorhinophalangeal syndrome type I | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
|
