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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
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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: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:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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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:0110728 | neuronal ceroid lipofuscinosis 5 | HGNC:2076 | Homo sapiens (human) | 1203 | CLN5 |
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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:0050775 | schneckenbecken dysplasia | HGNC:20800 | Homo sapiens (human) | 23169 | SLC35D1 |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | HGNC:20858 | Homo sapiens (human) | 23516 | SLC39A14 |
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| DOID:0060480 | left ventricular noncompaction | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| 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:594 | panic disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:9975 | cocaine dependence | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:2030 | anxiety disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:397 | restrictive cardiomyopathy | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
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| DOID:9970 | obesity | HGNC:21298 | Homo sapiens (human) | 65985 | AACS |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:21304 | Homo sapiens (human) | 54936 | ADPRS |
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