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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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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:0060001 | withdrawal disorder | HGNC:9595 | Homo sapiens (human) | 5733 | PTGER3 |
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| DOID:0060001 | withdrawal disorder | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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| DOID:0060001 | withdrawal disorder | RGD:69426 | Rattus norvegicus (Norway rat) | 29335 | Oprk1 |
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| DOID:0060001 | withdrawal disorder | HGNC:5286 | Homo sapiens (human) | 3350 | HTR1A |
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| DOID:0060001 | withdrawal disorder | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:0060001 | withdrawal disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0060001 | withdrawal disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0112171 | wrinkly skin syndrome | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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| DOID:0112171 | wrinkly skin syndrome | WB:WBGene00006916 | Caenorhabditis elegans | 178219 | vha-7 |
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| DOID:0112171 | wrinkly skin syndrome | WB:WBGene00006915 | Caenorhabditis elegans | 174743 | vha-6 |
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| DOID:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0112171 | wrinkly skin syndrome | MGI:104855 | Mus musculus (house mouse) | 21871 | Atp6v0a2 |
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| DOID:0070453 | xanthinuria type II | HGNC:18234 | Homo sapiens (human) | 55034 | MOCOS |
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| DOID:3345 | xanthomatosis | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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| DOID:3345 | xanthomatosis | HGNC:6547 | Homo sapiens (human) | 3949 | LDLR |
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| DOID:3345 | xanthomatosis | MGI:96765 | Mus musculus (house mouse) | 16835 | Ldlr |
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| DOID:3345 | xanthomatosis | RGD:2998 | Rattus norvegicus (Norway rat) | 300438 | Ldlr |
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| DOID:0050427 | xeroderma pigmentosum | SGD:S000002827 | Saccharomyces cerevisiae S288C | 852028 | RAD30 |
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| DOID:0050427 | xeroderma pigmentosum | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:0050427 | xeroderma pigmentosum | HGNC:11729 | Homo sapiens (human) | 7014 | TERF2 |
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| DOID:0050427 | xeroderma pigmentosum | HGNC:2717 | Homo sapiens (human) | 1642 | DDB1 |
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| DOID:0050427 | xeroderma pigmentosum | MGI:1202384 | Mus musculus (house mouse) | 13194 | Ddb1 |
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| DOID:0050427 | xeroderma pigmentosum | HGNC:9181 | Homo sapiens (human) | 5429 | POLH |
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| DOID:0110844 | xeroderma pigmentosum group C | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:0110849 | xeroderma pigmentosum group G | HGNC:3437 | Homo sapiens (human) | 2073 | ERCC5 |
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