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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:0070472 | early-onset epilepsy 3 | HGNC:855 | Homo sapiens (human) | 527 | ATP6V0C |
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| DOID:1826 | epilepsy | HGNC:855 | Homo sapiens (human) | 527 | ATP6V0C |
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| DOID:3963 | thyroid gland carcinoma | HGNC:855 | Homo sapiens (human) | 527 | ATP6V0C |
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| DOID:14219 | renal tubular acidosis | HGNC:866 | Homo sapiens (human) | 50617 | ATP6V0A4 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:866 | Homo sapiens (human) | 50617 | ATP6V0A4 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:14219 | renal tubular acidosis | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:865 | Homo sapiens (human) | 535 | ATP6V0A1 |
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| DOID:14219 | renal tubular acidosis | HGNC:865 | Homo sapiens (human) | 535 | ATP6V0A1 |
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| DOID:0070390 | developmental and epileptic encephalopathy 104 | HGNC:865 | Homo sapiens (human) | 535 | ATP6V0A1 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060309 | syndromic X-linked intellectual disability | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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| DOID:10763 | hypertension | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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| DOID:5212 | congenital disorder of glycosylation | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:10763 | hypertension | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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| DOID:0112002 | immunodeficiency 47 | HGNC:868 | Homo sapiens (human) | 537 | ATP6AP1 |
|
