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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:0111214 | autosomal recessive distal hereditary motor neuronopathy 5 | HGNC:5228 | Homo sapiens (human) | 3300 | DNAJB2 |
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| DOID:0080586 | Van Maldergem syndrome 2 | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:0080309 | fatal infantile hypertonic myofibrillar myopathy | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:0050941 | spastic ataxia 2 | HGNC:6317 | Homo sapiens (human) | 10749 | KIF1C |
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| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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| DOID:1324 | lung cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0110065 | amelogenesis imperfecta type 1F | HGNC:452 | Homo sapiens (human) | 258 | AMBN |
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| DOID:0060372 | Parkinson's disease 15 | HGNC:13586 | Homo sapiens (human) | 25793 | FBXO7 |
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| DOID:0060438 | Cole-Carpenter syndrome | HGNC:10706 | Homo sapiens (human) | 9871 | SEC24D |
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| DOID:0070065 | autosomal dominant intellectual developmental disorder 35 | HGNC:9312 | Homo sapiens (human) | 5528 | PPP2R5D |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | HGNC:4327 | Homo sapiens (human) | 2742 | GLRA2 |
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| DOID:0110264 | cataract 33 | HGNC:1040 | Homo sapiens (human) | 631 | BFSP1 |
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| DOID:0111839 | congenital disorder of glycosylation Icc | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:10871 | age related macular degeneration | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:0080059 | autosomal recessive spinocerebellar ataxia 7 | HGNC:2073 | Homo sapiens (human) | 1200 | TPP1 |
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| DOID:0081237 | acromesomelic dysplasia-3 | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:0060298 | complement component 4b deficiency | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0080987 | Ehlers-Danlos syndrome periodontal type 2 | HGNC:1247 | Homo sapiens (human) | 716 | C1S |
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| DOID:13096 | Sneddon syndrome | HGNC:1839 | Homo sapiens (human) | 51816 | ADA2 |
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| DOID:0112000 | immunodeficiency 34 | HGNC:2578 | Homo sapiens (human) | 1536 | CYBB |
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| DOID:7148 | rheumatoid arthritis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0111373 | familial progressive hyperpigmentation with or without hypopigmentation | HGNC:6343 | Homo sapiens (human) | 4254 | KITLG |
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