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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:0080944 | familial Behcet-like autoinflammatory syndrome | HGNC:11896 | Homo sapiens (human) | 7128 | TNFAIP3 |
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| DOID:0111144 | preterm premature rupture of the membranes | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0060197 | amyotrophic lateral sclerosis type 5 | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:2689 | Homo sapiens (human) | 1621 | DBH |
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| DOID:1580 | diffuse scleroderma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:10652 | Alzheimer's disease | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:848 | arthritis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0110393 | retinitis pigmentosa 66 | HGNC:9921 | Homo sapiens (human) | 5949 | RBP3 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:6693 | Homo sapiens (human) | 53353 | LRP1B |
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| DOID:14502 | cholesterol ester storage disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:10322 | berylliosis | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0080689 | mosaic variegated aneuploidy syndrome 3 | HGNC:12307 | Homo sapiens (human) | 9319 | TRIP13 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:13929 | lacrimal duct obstruction | HGNC:5950 | Homo sapiens (human) | 3321 | IGSF3 |
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| DOID:5723 | optic atrophy | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:0080591 | Klippel-Feil syndrome 3 | HGNC:4218 | Homo sapiens (human) | 9573 | GDF3 |
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| DOID:0080464 | developmental and epileptic encephalopathy 53 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0081226 | autosomal recessive intellectual developmental disorder 65 | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:0070093 | schizophrenia 18 | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:2841 | asthma | HGNC:15634 | Homo sapiens (human) | 81793 | TLR10 |
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| DOID:8923 | skin melanoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:0111650 | ectodermal dysplasia 13 | HGNC:17550 | Homo sapiens (human) | 83999 | KREMEN1 |
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| DOID:12132 | granulomatosis with polyangiitis | HGNC:3608 | Homo sapiens (human) | 2204 | FCAR |
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