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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:3672 | rhabdoid cancer | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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| DOID:14735 | hereditary angioedema | HGNC:9071 | Homo sapiens (human) | 5340 | PLG |
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| DOID:0111257 | gamma-glutamyl transpeptidase deficiency | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:0060335 | autosomal dominant sideroblastic anemia 4 | HGNC:5244 | Homo sapiens (human) | 3313 | HSPA9 |
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| DOID:0050636 | familial visceral amyloidosis | HGNC:3661 | Homo sapiens (human) | 2243 | FGA |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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| DOID:0112350 | spermatogenic failure 61 | HGNC:11356 | Homo sapiens (human) | 10734 | STAG3 |
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| DOID:0110386 | retinitis pigmentosa 42 | HGNC:15646 | Homo sapiens (human) | 55975 | KLHL7 |
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| DOID:1554 | vibratory urticaria | HGNC:3337 | Homo sapiens (human) | 30817 | ADGRE2 |
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| DOID:0070209 | hereditary lymphedema ID | HGNC:12682 | Homo sapiens (human) | 7424 | VEGFC |
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| DOID:9410 | panhypopituitarism | HGNC:18666 | Homo sapiens (human) | 55599 | RNPC3 |
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| DOID:0080058 | autosomal recessive spinocerebellar ataxia 14 | HGNC:11276 | Homo sapiens (human) | 6712 | SPTBN2 |
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| DOID:0080082 | nonsyndromic congenital nail disorder 4 | HGNC:16175 | Homo sapiens (human) | 343637 | RSPO4 |
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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:0070283 | primary autosomal recessive microcephaly 13 | HGNC:1856 | Homo sapiens (human) | 1062 | CENPE |
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| DOID:0060358 | multiple acyl-CoA dehydrogenase deficiency | HGNC:3482 | Homo sapiens (human) | 2109 | ETFB |
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| DOID:0110351 | osteogenesis imperfecta type 11 | HGNC:18169 | Homo sapiens (human) | 60681 | FKBP10 |
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| DOID:0112259 | Leydig cell hypoplasia | HGNC:6585 | Homo sapiens (human) | 3973 | LHCGR |
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| DOID:0110711 | congenital hypotrichosis with juvenile macular dystrophy | HGNC:1762 | Homo sapiens (human) | 1001 | CDH3 |
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| DOID:14735 | hereditary angioedema | HGNC:484 | Homo sapiens (human) | 284 | ANGPT1 |
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| DOID:0111202 | autosomal dominant distal hereditary motor neuronopathy 14 | HGNC:2711 | Homo sapiens (human) | 1639 | DCTN1 |
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| DOID:0080688 | mosaic variegated aneuploidy syndrome | HGNC:20465 | Homo sapiens (human) | 23137 | SMC5 |
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| DOID:0070441 | retinal macular dystrophy 4 | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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