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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
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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:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0110645 | long QT syndrome 2 | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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| DOID:0050563 | nonsyndromic deafness | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | HGNC:30881 | Homo sapiens (human) | 79868 | ALG13 |
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| DOID:9970 | obesity | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:0050729 | Chanarin-Dorfman syndrome | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:0060158 | acquired metabolic disease | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0080573 | congenital disorder of glycosylation Ix | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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| DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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| DOID:162 | cancer | HGNC:30596 | Homo sapiens (human) | 80235 | PIGZ |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:2377 | multiple sclerosis | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:3328 | temporal lobe epilepsy | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:11446 | sciatic neuropathy | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:3525 | middle cerebral artery infarction | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:10283 | prostate cancer | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:104 | bacterial infectious disease | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:162 | cancer | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:8893 | psoriasis | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:3407 | carotid artery disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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