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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
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:0111364 | Alzheimer's disease 9 | HGNC:37 | Homo sapiens (human) | 10347 | ABCA7 |
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| DOID:0111123 | nephronophthisis 15 | HGNC:29182 | Homo sapiens (human) | 22897 | CEP164 |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:13861 | Homo sapiens (human) | 11178 | LZTS1 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0060821 | syndromic X-linked intellectual disability 14 | HGNC:20439 | Homo sapiens (human) | 65109 | UPF3B |
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| DOID:0080589 | Klippel-Feil syndrome 1 | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
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| DOID:2747 | glycogen storage disease | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:9256 | colorectal cancer | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0080924 | bilateral perisylvian polymicrogyria | HGNC:4512 | Homo sapiens (human) | 9289 | ADGRG1 |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:0111180 | French Canadian Leigh disease | HGNC:15714 | Homo sapiens (human) | 10128 | LRPPRC |
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| DOID:0060838 | isolated microphthalmia 7 | HGNC:4218 | Homo sapiens (human) | 9573 | GDF3 |
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| DOID:0060203 | amyotrophic lateral sclerosis type 12 | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:0111649 | ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome | HGNC:1762 | Homo sapiens (human) | 1001 | CDH3 |
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| DOID:0111437 | optic atrophy 7 | HGNC:25382 | Homo sapiens (human) | 84233 | TMEM126A |
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| DOID:0080339 | familial erythrocytosis 4 | HGNC:3374 | Homo sapiens (human) | 2034 | EPAS1 |
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| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:30348 | Homo sapiens (human) | 55703 | POLR3B |
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| DOID:0080560 | congenital disorder of glycosylation Ih | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0111059 | Bernard-Soulier syndrome type A2 | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
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| DOID:0111310 | familial febrile seizures 2 | HGNC:4846 | Homo sapiens (human) | 610 | HCN2 |
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| DOID:9007 | sudden infant death syndrome | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:0060571 | Ritscher-Schinzel syndrome 1 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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