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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:2394 | ovarian cancer | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:684 | hepatocellular carcinoma | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:13810 | familial hypercholesterolemia | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:0081223 | glycosylphosphatidylinositol biosynthesis defect 16 | HGNC:8960 | Homo sapiens (human) | 5279 | PIGC |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:8719 | in situ carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:1289 | neurodegenerative disease | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:10907 | microcephaly | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:1059 | intellectual disability | HGNC:20779 | Homo sapiens (human) | 64579 | NDST4 |
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| DOID:12800 | mucopolysaccharidosis VI | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:783 | end stage renal disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:14330 | Parkinson's disease | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:9256 | colorectal cancer | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:3393 | coronary artery disease | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:1909 | melanoma | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:5679 | retinal disease | HGNC:9059 | Homo sapiens (human) | 5332 | PLCB4 |
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| DOID:2527 | nephrosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:2030 | anxiety disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:1070 | primary open angle glaucoma | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:3070 | high grade glioma | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:0111394 | mucopolysaccharidosis type IIIB | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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