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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:0110375 | retinitis pigmentosa 40 | HGNC:8786 | Homo sapiens (human) | 5158 | PDE6B |
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| DOID:0060537 | mitochondrial complex II deficiency | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:0060479 | Shwachman-Diamond syndrome | HGNC:25789 | Homo sapiens (human) | 79631 | EFL1 |
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| DOID:0111457 | STING-associated vasculopathy with onset in infancy | HGNC:27962 | Homo sapiens (human) | 340061 | STING1 |
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| DOID:0060730 | torsion dystonia 1 | HGNC:3098 | Homo sapiens (human) | 1861 | TOR1A |
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| DOID:0110773 | hereditary spastic paraplegia 2 | HGNC:9086 | Homo sapiens (human) | 5354 | PLP1 |
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| DOID:0090018 | autosomal dominant familial periodic fever | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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| DOID:0111668 | Kohlschutter-Tonz syndrome | HGNC:29478 | Homo sapiens (human) | 79641 | ROGDI |
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| DOID:0110726 | neuronal ceroid lipofuscinosis 2 | HGNC:2073 | Homo sapiens (human) | 1200 | TPP1 |
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| DOID:0111011 | cone-rod dystrophy 6 | HGNC:4689 | Homo sapiens (human) | 3000 | GUCY2D |
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| DOID:2394 | ovarian cancer | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
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| DOID:0060356 | Vici syndrome | HGNC:29331 | Homo sapiens (human) | 57724 | EPG5 |
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| DOID:0080506 | Cornelia de Lange syndrome 2 | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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| DOID:0110765 | hereditary spastic paraplegia 12 | HGNC:10468 | Homo sapiens (human) | 6253 | RTN2 |
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| DOID:0110893 | inflammatory bowel disease 13 | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:0110471 | autosomal recessive nonsyndromic deafness 16 | HGNC:16035 | Homo sapiens (human) | 161497 | STRC |
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| DOID:0110266 | cataract 9 multiple types | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:0060832 | Griscelli syndrome type 1 | HGNC:7602 | Homo sapiens (human) | 4644 | MYO5A |
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| DOID:0110340 | osteogenesis imperfecta type 4 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0110668 | congenital myasthenic syndrome 10 | HGNC:26594 | Homo sapiens (human) | 285489 | DOK7 |
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| DOID:0111496 | combined oxidative phosphorylation deficiency 17 | HGNC:14198 | Homo sapiens (human) | 60528 | ELAC2 |
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| DOID:0050711 | aceruloplasminemia | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:0080387 | nephrotic syndrome type 12 | HGNC:28958 | Homo sapiens (human) | 9688 | NUP93 |
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| DOID:8398 | osteoarthritis | HGNC:6909 | Homo sapiens (human) | 4148 | MATN3 |
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