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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: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: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:0081097 | Rafiq syndrome | HGNC:6823 | Homo sapiens (human) | 11253 | MAN1B1 |
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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: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: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:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
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| DOID:1793 | pancreatic cancer | HGNC:7047 | Homo sapiens (human) | 11320 | MGAT4A |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:87867 | Mus musculus (house mouse) | 11364 | Acadm |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | MGI:87867 | Mus musculus (house mouse) | 11364 | Acadm |
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| DOID:10325 | silicosis | RGD:1303058 | Rattus norvegicus (Norway rat) | 113901 | Chia |
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| DOID:12053 | cryptococcosis | RGD:1303058 | Rattus norvegicus (Norway rat) | 113901 | Chia |
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| DOID:0050127 | sinusitis | RGD:1303058 | Rattus norvegicus (Norway rat) | 113901 | Chia |
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| DOID:2841 | asthma | RGD:1303058 | Rattus norvegicus (Norway rat) | 113901 | Chia |
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