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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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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:3459 | breast carcinoma | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:83 | cataract | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:219 | colon cancer | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:3181 | oligodendroglioma | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
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| DOID:0060668 | anencephaly | HGNC:3225 | Homo sapiens (human) | 1946 | EFNA5 |
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| DOID:5844 | myocardial infarction | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:13317 | hyperinsulinemic hypoglycemia | HGNC:4925 | Homo sapiens (human) | 3101 | HK3 |
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| DOID:0110915 | childhood hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:12849 | autistic disorder | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:13580 | cholestasis | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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| DOID:6432 | pulmonary hypertension | HGNC:5321 | Homo sapiens (human) | 8692 | HYAL2 |
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| DOID:446 | primary hyperaldosteronism | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:9281 | phenylketonuria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0080784 | urinary tract infection | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:4448 | macular degeneration | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:114 | heart disease | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:2394 | ovarian cancer | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0060475 | myoclonic-atonic epilepsy | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0014667 | disease of metabolism | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:10534 | stomach cancer | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:9261 | nasopharynx carcinoma | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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| DOID:552 | pneumonia | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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