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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:3493 | signet ring cell adenocarcinoma | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:1380 | endometrial cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:2671 | transitional cell carcinoma | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:10808 | gastric ulcer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:2394 | ovarian cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:3702 | cervical adenocarcinoma | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:0060180 | colitis | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:10283 | prostate cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:11054 | urinary bladder cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:10534 | stomach cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:0080365 | endometrial hyperplasia | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:13550 | angle-closure glaucoma | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:535 | sleep disorder | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:13832 | patent ductus arteriosus | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:0060563 | Char syndrome | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:13268 | porphyria | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:1724 | duodenal ulcer | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:10763 | hypertension | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:3526 | cerebral infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0060903 | thrombosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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