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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:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:26789 | Homo sapiens (human) | 144811 | LACC1 |
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| DOID:2394 | ovarian cancer | HGNC:8143 | Homo sapiens (human) | 4978 | OPCML |
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| DOID:0080844 | omodysplasia 1 | HGNC:4454 | Homo sapiens (human) | 10082 | GPC6 |
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| DOID:0111232 | congenital muscular dystrophy-dystroglycanopathy type A9 | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0090141 | cortisone reductase deficiency 1 | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:0111646 | congenital lactase deficiency | HGNC:6530 | Homo sapiens (human) | 3938 | LCT |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0112147 | retinitis pigmentosa 90 | HGNC:5384 | Homo sapiens (human) | 3419 | IDH3A |
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| DOID:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0070399 | hypomyelinating leukodystrophy 18 | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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| DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:0080488 | mucolipidosis | HGNC:7758 | Homo sapiens (human) | 4758 | NEU1 |
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| DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:6498 | seborrheic keratosis | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0080573 | congenital disorder of glycosylation Ix | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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