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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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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:0050994 | episodic ataxia type 6 | HGNC:10943 | Homo sapiens (human) | 6510 | SLC1A5 |
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| DOID:1826 | epilepsy | HGNC:10943 | Homo sapiens (human) | 6510 | SLC1A5 |
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| DOID:1289 | neurodegenerative disease | HGNC:10943 | Homo sapiens (human) | 6510 | SLC1A5 |
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| DOID:0050994 | episodic ataxia type 6 | HGNC:10942 | Homo sapiens (human) | 6509 | SLC1A4 |
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| DOID:1826 | epilepsy | HGNC:10942 | Homo sapiens (human) | 6509 | SLC1A4 |
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| DOID:0070537 | spastic tetraplegia, thin corpus callosum, and progressive microcephaly | HGNC:10942 | Homo sapiens (human) | 6509 | SLC1A4 |
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| DOID:1289 | neurodegenerative disease | HGNC:10942 | Homo sapiens (human) | 6509 | SLC1A4 |
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| DOID:1289 | neurodegenerative disease | HGNC:10941 | Homo sapiens (human) | 6507 | SLC1A3 |
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| DOID:0050994 | episodic ataxia type 6 | HGNC:10941 | Homo sapiens (human) | 6507 | SLC1A3 |
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| DOID:1826 | epilepsy | HGNC:10941 | Homo sapiens (human) | 6507 | SLC1A3 |
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| DOID:13544 | low tension glaucoma | HGNC:10941 | Homo sapiens (human) | 6507 | SLC1A3 |
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| DOID:0080442 | developmental and epileptic encephalopathy 41 | HGNC:10940 | Homo sapiens (human) | 6506 | SLC1A2 |
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| DOID:1289 | neurodegenerative disease | HGNC:10940 | Homo sapiens (human) | 6506 | SLC1A2 |
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| DOID:12858 | Huntington's disease | HGNC:10940 | Homo sapiens (human) | 6506 | SLC1A2 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:10940 | Homo sapiens (human) | 6506 | SLC1A2 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:10940 | Homo sapiens (human) | 6506 | SLC1A2 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:1094 | Homo sapiens (human) | 670 | BPHL |
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| DOID:1289 | neurodegenerative disease | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:0050994 | episodic ataxia type 6 | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:1826 | epilepsy | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:4752 | multiple system atrophy | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:13544 | low tension glaucoma | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:0060650 | dicarboxylic aminoaciduria | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:0070093 | schizophrenia 18 | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:0090117 | thiamine-responsive megaloblastic anemia syndrome | HGNC:10938 | Homo sapiens (human) | 10560 | SLC19A2 |
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