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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:9119 | acute myeloid leukemia | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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| DOID:0080596 | hyper IgE recurrent infection syndrome 4 | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:8778 | Crohn's disease | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:1588 | thrombocytopenia | HGNC:11283 | Homo sapiens (human) | 6714 | SRC |
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| DOID:0110831 | Usher syndrome type 1D | HGNC:14674 | Homo sapiens (human) | 65217 | PCDH15 |
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| DOID:0080688 | mosaic variegated aneuploidy syndrome | HGNC:17814 | Homo sapiens (human) | 55719 | SLF2 |
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| DOID:0060752 | familial temporal lobe epilepsy 5 | HGNC:17245 | Homo sapiens (human) | 57094 | CPA6 |
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| DOID:0110682 | congenital myasthenic syndrome 16 | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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| DOID:0080608 | anterior segment dysgenesis 3 | HGNC:3800 | Homo sapiens (human) | 2296 | FOXC1 |
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| DOID:0112137 | combined oxidative phosphorylation deficiency 51 | HGNC:24717 | Homo sapiens (human) | 55037 | PTCD3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:7562 | Homo sapiens (human) | 4615 | MYD88 |
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| DOID:0111347 | epidermolysis bullosa with congenital localized absence of skin and deformity of nails | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0081215 | autosomal recessive intellectual developmental disorder 52 | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0081340 | congenital myopathy 2C | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081163 | dilated cardiomyopathy 2G | HGNC:6648 | Homo sapiens (human) | 442721 | LMOD2 |
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| DOID:0080265 | nephrotic syndrome type 14 | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:3236 | Homo sapiens (human) | 1956 | EGFR |
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| DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:0112127 | HRPT-related hyperuricemia | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:0080061 | autosomal recessive spinocerebellar ataxia 2 | HGNC:18667 | Homo sapiens (human) | 23203 | PMPCA |
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