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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070491 | mitochondrial complex IV deficiency nuclear type 1 | HGNC:11474 | Homo sapiens (human) | 6834 | SURF1 |
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| DOID:0060676 | catecholaminergic polymorphic ventricular tachycardia 2 | HGNC:1513 | Homo sapiens (human) | 845 | CASQ2 |
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| DOID:9970 | obesity | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:8947 | diabetic retinopathy | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:11054 | urinary bladder cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:9256 | colorectal cancer | HGNC:11283 | Homo sapiens (human) | 6714 | SRC |
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| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:1206 | Rett syndrome | HGNC:6990 | Homo sapiens (human) | 4204 | MECP2 |
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| DOID:0110195 | Charcot-Marie-Tooth disease type 4E | HGNC:3239 | Homo sapiens (human) | 1959 | EGR2 |
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| DOID:0050437 | Danon disease | HGNC:6501 | Homo sapiens (human) | 3920 | LAMP2 |
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| DOID:0050948 | autosomal dominant hypophosphatemic rickets | HGNC:3680 | Homo sapiens (human) | 8074 | FGF23 |
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| DOID:3322 | GM1 gangliosidosis | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0060349 | microcephaly with or without chorioretinopathy, lymphedema, or mental retardation | HGNC:6388 | Homo sapiens (human) | 3832 | KIF11 |
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| DOID:0110074 | arrhythmogenic right ventricular dysplasia 5 | HGNC:28472 | Homo sapiens (human) | 79188 | TMEM43 |
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| DOID:0080394 | nephrotic syndrome type 19 | HGNC:18017 | Homo sapiens (human) | 23279 | NUP160 |
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| DOID:0110735 | neurodegeneration with brain iron accumulation 2a | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:2349 | arteriosclerosis | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0110354 | retinitis pigmentosa 19 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:3652 | Leigh disease | HGNC:11474 | Homo sapiens (human) | 6834 | SURF1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7873 | Homo sapiens (human) | 4843 | NOS2 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:627 | severe combined immunodeficiency | HGNC:6010 | Homo sapiens (human) | 3561 | IL2RG |
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| DOID:0090120 | hereditary neutrophilia | HGNC:2439 | Homo sapiens (human) | 1441 | CSF3R |
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| DOID:0110792 | hereditary spastic paraplegia 4 | HGNC:11233 | Homo sapiens (human) | 6683 | SPAST |
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