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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050734 | congenital intrinsic factor deficiency | HGNC:4268 | Homo sapiens (human) | 2694 | CBLIF |
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| DOID:11713 | diabetic angiopathy | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:1394 | urinary schistosomiasis | HGNC:11368 | Homo sapiens (human) | 6778 | STAT6 |
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| DOID:14499 | Fabry disease | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:0050974 | spinocerebellar ataxia type 25 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
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| DOID:7147 | ankylosing spondylitis | HGNC:25240 | Homo sapiens (human) | 196527 | ANO6 |
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| DOID:0081396 | neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome | HGNC:25567 | Homo sapiens (human) | 55210 | ATAD3A |
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| DOID:1070 | primary open angle glaucoma | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:11904 | Homo sapiens (human) | 8797 | TNFRSF10A |
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| DOID:5844 | myocardial infarction | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
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| DOID:0060450 | Lisch epithelial corneal dystrophy | HGNC:13356 | Homo sapiens (human) | 57192 | MCOLN1 |
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| DOID:0060303 | complement component 9 deficiency | HGNC:1358 | Homo sapiens (human) | 735 | C9 |
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| DOID:655 | inherited metabolic disorder | HGNC:15465 | Homo sapiens (human) | 10243 | GPHN |
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| DOID:0110541 | autosomal dominant nonsyndromic deafness 1 | HGNC:2876 | Homo sapiens (human) | 1729 | DIAPH1 |
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| DOID:321 | tropical spastic paraparesis | HGNC:7794 | Homo sapiens (human) | 4790 | NFKB1 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0060811 | syndromic X-linked intellectual disability Turner type | HGNC:30892 | Homo sapiens (human) | 10075 | HUWE1 |
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| DOID:2352 | hemochromatosis | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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| DOID:3312 | bipolar disorder | HGNC:11334 | Homo sapiens (human) | 6755 | SSTR5 |
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| DOID:10608 | celiac disease | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:5844 | myocardial infarction | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:12365 | malaria | HGNC:19077 | Homo sapiens (human) | 259197 | NCR3 |
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