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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:1793 | pancreatic cancer | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:10211 | cholelithiasis | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:11265 | trachoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4481 | allergic rhinitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2977 | primary hyperoxaluria | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:4621 | holoprosencephaly | HGNC:29185 | Homo sapiens (human) | 23007 | PLCH1 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:5844 | myocardial infarction | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:10763 | hypertension | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:552 | pneumonia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:3407 | carotid artery disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:13564 | aspergillosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:1070 | primary open angle glaucoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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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:9970 | obesity | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:1059 | intellectual disability | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:2841 | asthma | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:8618 | oral cavity cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:670 | amphetamine abuse | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:12361 | Graves' disease | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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