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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0112240 | Leber congenital amaurosis with early-onset deafness | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
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| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0111134 | focal segmental glomerulosclerosis 9 | HGNC:18688 | Homo sapiens (human) | 286204 | CRB2 |
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| DOID:0110204 | Charcot-Marie-Tooth disease recessive intermediate B | HGNC:6215 | Homo sapiens (human) | 3735 | KARS1 |
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| DOID:0080661 | nonsyndromic aplasia cutis congenita | HGNC:23505 | Homo sapiens (human) | 9790 | BMS1 |
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| DOID:0060944 | episodic kinesigenic dyskinesia 3 | HGNC:28497 | Homo sapiens (human) | 256472 | TMEM151A |
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| DOID:0070525 | peeling skin syndrome 6 | HGNC:33276 | Homo sapiens (human) | 388698 | FLG2 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:17601 | Homo sapiens (human) | 57863 | CADM3 |
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| DOID:0060209 | amyotrophic lateral sclerosis type 18 | HGNC:8881 | Homo sapiens (human) | 5216 | PFN1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:11825 | Homo sapiens (human) | 7080 | NKX2-1 |
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| DOID:0090076 | hypogonadotropic hypogonadism 18 with or without anosmia | HGNC:17616 | Homo sapiens (human) | 54756 | IL17RD |
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| DOID:0080231 | autosomal dominant intellectual developmental disorder 52 | HGNC:19088 | Homo sapiens (human) | 55870 | ASH1L |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:0081424 | familial focal epilepsy with variable foci 4 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0111841 | Shukla-Vernon syndrome | HGNC:25657 | Homo sapiens (human) | 63035 | BCORL1 |
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| DOID:0050641 | Rh deficiency syndrome | HGNC:10006 | Homo sapiens (human) | 6005 | RHAG |
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| DOID:0080787 | proximal symphalangism 1 | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:0111331 | intellectual disability-severe speech delay-mild dysmorphism syndrome | HGNC:3823 | Homo sapiens (human) | 27086 | FOXP1 |
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| DOID:0111363 | Heinz body anemia | HGNC:4823 | Homo sapiens (human) | 3039 | HBA1 |
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| DOID:0080631 | Elsahy-Waters syndrome | HGNC:1750 | Homo sapiens (human) | 1009 | CDH11 |
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| DOID:0110357 | retinitis pigmentosa 35 | HGNC:10729 | Homo sapiens (human) | 64218 | SEMA4A |
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| DOID:0080065 | autosomal recessive spinocerebellar ataxia 19 | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:0110217 | Leber congenital amaurosis 17 | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:11842 | Homo sapiens (human) | 11011 | TLK2 |
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| DOID:0080434 | developmental and epileptic encephalopathy 61 | HGNC:201 | Homo sapiens (human) | 53616 | ADAM22 |
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