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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
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:0080046 | Stickler syndrome | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:8398 | osteoarthritis | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0080675 | Stickler syndrome 2 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0080021 | Schmid metaphyseal chondrodysplasia | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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| DOID:90 | degenerative disc disease | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | SGD:S000004536 | Saccharomyces cerevisiae S288C | 854904 | COG8 |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:630 | genetic disease | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | SGD:S000004986 | Saccharomyces cerevisiae S288C | 855687 | COG6 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | SGD:S000004996 | Saccharomyces cerevisiae S288C | 855676 | COG5 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | SGD:S000006309 | Saccharomyces cerevisiae S288C | 856220 | COG4 |
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| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0111673 | Saul-Wilson syndrome | SGD:S000006309 | Saccharomyces cerevisiae S288C | 856220 | COG4 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18619 | Homo sapiens (human) | 83548 | COG3 |
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| DOID:0050571 | congenital disorder of glycosylation type II | SGD:S000000959 | Saccharomyces cerevisiae S288C | 856901 | COG3 |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
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| DOID:0111644 | autosomal recessive nonsyndromic deafness 110 | HGNC:2180 | Homo sapiens (human) | 1690 | COCH |
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| DOID:0110593 | autosomal dominant nonsyndromic deafness 9 | HGNC:2180 | Homo sapiens (human) | 1690 | COCH |
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