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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:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:0060250 | idiopathic scoliosis | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | HGNC:20858 | Homo sapiens (human) | 23516 | SLC39A14 |
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| DOID:0050775 | schneckenbecken dysplasia | HGNC:20800 | Homo sapiens (human) | 23169 | SLC35D1 |
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| DOID:14227 | azoospermia | HGNC:20779 | Homo sapiens (human) | 64579 | NDST4 |
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| DOID:0060041 | autism spectrum disorder | HGNC:20779 | Homo sapiens (human) | 64579 | NDST4 |
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| DOID:1059 | intellectual disability | HGNC:20779 | Homo sapiens (human) | 64579 | NDST4 |
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| DOID:0110728 | neuronal ceroid lipofuscinosis 5 | HGNC:2076 | Homo sapiens (human) | 1203 | CLN5 |
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| DOID:162 | cancer | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:10763 | hypertension | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:5844 | myocardial infarction | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:11714 | gestational diabetes | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:10591 | pre-eclampsia | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:4248 | coronary stenosis | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0080887 | vitamin D-dependent rickets type 1B | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:3393 | coronary artery disease | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:3454 | brain infarction | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:9970 | obesity | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:10763 | hypertension | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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