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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:5844 | myocardial infarction | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:4079 | heart valve disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8893 | psoriasis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:905 | Zellweger syndrome | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:9970 | obesity | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:1074 | kidney failure | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:1289 | neurodegenerative disease | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0050745 | diffuse large B-cell lymphoma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0014667 | disease of metabolism | HGNC:21481 | Homo sapiens (human) | 92483 | LDHAL6B |
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| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:1826 | epilepsy | HGNC:24649 | Homo sapiens (human) | 55500 | ETNK1 |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:10941 | intracranial aneurysm | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12895 | keratoconjunctivitis sicca | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4926 | bronchiolo-alveolar adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9119 | acute myeloid leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:1852 | intrahepatic cholestasis | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:0050741 | alcohol dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9119 | acute myeloid leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:557 | kidney disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:0050848 | obstructive sleep apnea | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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