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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:0110820 | hereditary spastic paraplegia 75 | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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| DOID:2841 | asthma | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0080365 | endometrial hyperplasia | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:3069 | malignant astrocytoma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:11446 | sciatic neuropathy | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:11832 | visual epilepsy | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18619 | Homo sapiens (human) | 83548 | COG3 |
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| DOID:1459 | hypothyroidism | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:3459 | breast carcinoma | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:14735 | hereditary angioedema | HGNC:14178 | Homo sapiens (human) | 64711 | HS3ST6 |
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| DOID:14766 | renal agenesis | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:2841 | asthma | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:7147 | ankylosing spondylitis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:224 | transient cerebral ischemia | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:0081337 | congenital myopathy | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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| DOID:9471 | meningitis | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:2560 | morphine dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:10763 | hypertension | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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