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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:9119 | acute myeloid leukemia | MGI:87859 | Mus musculus (house mouse) | 11350 | Abl1 |
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| DOID:4914 | esophagus adenocarcinoma | MGI:87859 | Mus musculus (house mouse) | 11350 | Abl1 |
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| DOID:9256 | colorectal cancer | MGI:87859 | Mus musculus (house mouse) | 11350 | Abl1 |
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| DOID:5199 | ureteral obstruction | MGI:87859 | Mus musculus (house mouse) | 11350 | Abl1 |
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| DOID:0050866 | oral squamous cell carcinoma | MGI:87859 | Mus musculus (house mouse) | 11350 | Abl1 |
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| DOID:0060685 | autosomal dominant nocturnal frontal lobe epilepsy 4 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:1574 | alcohol use disorder | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:0081119 | benign familial infantile seizures 6 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:784 | chronic kidney disease | HGNC:30672 | Homo sapiens (human) | 11346 | SYNPO |
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| DOID:0112209 | developmental and epileptic encephalopathy 73 | HGNC:10057 | Homo sapiens (human) | 11342 | RNF13 |
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| DOID:0112334 | pontocerebellar hypoplasia type 1C | HGNC:17035 | Homo sapiens (human) | 11340 | EXOSC8 |
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| DOID:1574 | alcohol use disorder | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:0110662 | congenital myasthenic syndrome 1B | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:0110663 | congenital myasthenic syndrome 1A | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:0060933 | developmental delay, dysmorphic facies, and brain anomalies | HGNC:23156 | Homo sapiens (human) | 11338 | U2AF2 |
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| DOID:0080785 | Brown-Vialetto-Van Laere syndrome 1 | HGNC:16187 | Homo sapiens (human) | 113278 | SLC52A3 |
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| DOID:0050694 | Brown-Vialetto-Van Laere syndrome | HGNC:16187 | Homo sapiens (human) | 113278 | SLC52A3 |
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| DOID:0080632 | Fazio-Londe disease | HGNC:16187 | Homo sapiens (human) | 113278 | SLC52A3 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:18676 | Homo sapiens (human) | 11325 | DDX42 |
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| DOID:0111678 | hereditary folate malabsorption | HGNC:30521 | Homo sapiens (human) | 113235 | SLC46A1 |
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| DOID:784 | chronic kidney disease | HGNC:30521 | Homo sapiens (human) | 113235 | SLC46A1 |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:18021 | Homo sapiens (human) | 11322 | TMC6 |
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| DOID:1793 | pancreatic cancer | HGNC:7047 | Homo sapiens (human) | 11320 | MGAT4A |
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