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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:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:10763 | hypertension | HGNC:2648 | Homo sapiens (human) | 11283 | CYP4F8 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:2648 | Homo sapiens (human) | 11283 | CYP4F8 |
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| DOID:2977 | primary hyperoxaluria | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0081097 | Rafiq syndrome | HGNC:6823 | Homo sapiens (human) | 11253 | MAN1B1 |
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| DOID:8619 | recurrent hypersomnia | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:9884 | muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:10907 | microcephaly | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:1059 | intellectual disability | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:1826 | epilepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:1826 | epilepsy | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:224 | transient cerebral ischemia | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:219 | colon cancer | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:10907 | microcephaly | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:0050912 | colon adenoma | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:1909 | melanoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:2349 | arteriosclerosis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0080199 | colorectal carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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