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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
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:0080855 | Parkinsonism | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:2548 | reflex epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0050562 | West syndrome | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:10763 | hypertension | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:1824 | status epilepticus | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:1596 | depressive disorder | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:10652 | Alzheimer's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:11832 | visual epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0060404 | chromosome 17q12 deletion syndrome | HGNC:19235 | Homo sapiens (human) | 26574 | AATF |
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| DOID:0111479 | combined oxidative phosphorylation deficiency 8 | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:10907 | microcephaly | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:7319 | axonal neuropathy | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:0070396 | progressive leukoencephalopathy with ovarian failure | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:10223 | dermatomyositis | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:0050753 | cerebellar ataxia | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:0111866 | trichothiodystrophy | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:10579 | leukodystrophy | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:0110177 | Charcot-Marie-Tooth disease axonal type 2N | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:0080451 | developmental and epileptic encephalopathy 29 | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:10223 | dermatomyositis | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:0050753 | cerebellar ataxia | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:7319 | axonal neuropathy | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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