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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:5419 | schizophrenia | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:4189 | mutism | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:1059 | intellectual disability | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:12849 | autistic disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060244 | specific language impairment | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:11832 | visual epilepsy | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:4186 | articulation disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0090130 | cortical dysplasia-focal epilepsy syndrome | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:0080365 | endometrial hyperplasia | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:3459 | breast carcinoma | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:4450 | renal cell carcinoma | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:3883 | Lynch syndrome | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:2043 | hepatitis B | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:11054 | urinary bladder cancer | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:2671 | transitional cell carcinoma | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:0111647 | Schopf-Schulz-Passarge syndrome | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:0050591 | tooth agenesis | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:2121 | ectodermal dysplasia | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:4239 | alveolar soft part sarcoma | HGNC:13825 | Homo sapiens (human) | 79058 | ASPSCR1 |
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| DOID:12236 | primary biliary cholangitis | HGNC:13819 | Homo sapiens (human) | 53919 | SLCO1C1 |
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| DOID:0111315 | idiopathic generalized epilepsy 14 | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
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| DOID:0080460 | developmental and epileptic encephalopathy 34 | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
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