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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:1380 | endometrial cancer | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:10211 | cholelithiasis | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:10966 | lipoid nephrosis | HGNC:6561 | Homo sapiens (human) | 3956 | LGALS1 |
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| DOID:3008 | invasive ductal carcinoma | HGNC:5210 | Homo sapiens (human) | 3292 | HSD17B1 |
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| DOID:11716 | prediabetes syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:8947 | diabetic retinopathy | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:11166 | Human papillomavirus infectious disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:11265 | trachoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10487 | Hirschsprung's disease | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:9452 | steatotic liver disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:106 | pleural tuberculosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9970 | obesity | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:6000 | congestive heart failure | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:4481 | allergic rhinitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:6432 | pulmonary hypertension | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:2977 | primary hyperoxaluria | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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| DOID:1891 | optic nerve disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:4621 | holoprosencephaly | HGNC:29185 | Homo sapiens (human) | 23007 | PLCH1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12858 | Huntington's disease | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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