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GlyTouCan
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:9280 | carbamoyl phosphate synthetase I deficiency disease | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:3247 | rhabdomyosarcoma | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:0050833 | orotic aciduria | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:0080419 | developmental and epileptic encephalopathy 50 | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:4450 | renal cell carcinoma | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:684 | hepatocellular carcinoma | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:9119 | acute myeloid leukemia | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:769 | neuroblastoma | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:225 | syndrome | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:10907 | microcephaly | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:0112103 | Sotos syndrome 1 | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:14748 | Sotos syndrome | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:0080236 | autosomal dominant intellectual developmental disorder 45 | HGNC:14214 | Homo sapiens (human) | 23152 | CIC |
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| DOID:150 | disease of mental health | HGNC:14214 | Homo sapiens (human) | 23152 | CIC |
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| DOID:0050700 | cardiomyopathy | HGNC:14201 | Homo sapiens (human) | 56704 | JPH1 |
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| DOID:0110167 | Charcot-Marie-Tooth disease axonal type 2K | HGNC:14201 | Homo sapiens (human) | 56704 | JPH1 |
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| DOID:0111496 | combined oxidative phosphorylation deficiency 17 | HGNC:14198 | Homo sapiens (human) | 60528 | ELAC2 |
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| DOID:10283 | prostate cancer | HGNC:14198 | Homo sapiens (human) | 60528 | ELAC2 |
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| DOID:0111753 | infantile hypertrophic cardiomyopathy | HGNC:14198 | Homo sapiens (human) | 60528 | ELAC2 |
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| DOID:0060536 | mitochondrial complex I deficiency | HGNC:14198 | Homo sapiens (human) | 60528 | ELAC2 |
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| DOID:0050700 | cardiomyopathy | HGNC:14198 | Homo sapiens (human) | 60528 | ELAC2 |
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| DOID:14735 | hereditary angioedema | HGNC:14178 | Homo sapiens (human) | 64711 | HS3ST6 |
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| DOID:0111422 | familial lipase maturation factor 1 deficiency | HGNC:14154 | Homo sapiens (human) | 64788 | LMF1 |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:1909 | melanoma | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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