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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
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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:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0080142 | mosaic variegated aneuploidy syndrome 2 | HGNC:30794 | Homo sapiens (human) | 9702 | CEP57 |
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| DOID:0080694 | Galloway-Mowat syndrome | HGNC:18016 | Homo sapiens (human) | 55746 | NUP133 |
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| DOID:0080287 | spinocerebellar ataxia 45 | HGNC:3596 | Homo sapiens (human) | 2196 | FAT2 |
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| DOID:0060342 | acromelic frontonasal dysostosis | HGNC:29316 | Homo sapiens (human) | 57688 | ZSWIM6 |
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| DOID:0090136 | complex cortical dysplasia with other brain malformations 6 | HGNC:20778 | Homo sapiens (human) | 203068 | TUBB |
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| DOID:0070391 | developmental and epileptic encephalopathy 105 | HGNC:15736 | Homo sapiens (human) | 283987 | HID1 |
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| DOID:0110971 | brachydactyly type D | HGNC:5136 | Homo sapiens (human) | 3239 | HOXD13 |
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| DOID:0111907 | thrombophilia due to thrombin defect | HGNC:4798 | Homo sapiens (human) | 3026 | HABP2 |
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| DOID:0111917 | spermatogenic failure 43 | HGNC:26293 | Homo sapiens (human) | 79925 | SPEF2 |
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| DOID:0111502 | combined oxidative phosphorylation deficiency 6 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0110014 | age related macular degeneration 1 | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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| DOID:0110663 | congenital myasthenic syndrome 1A | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:0111730 | familial episodic pain syndrome 2 | HGNC:10582 | Homo sapiens (human) | 6336 | SCN10A |
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| DOID:0070123 | congenital nongoitrous hypothyroidism 4 | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:0110699 | hypotrichosis 2 | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:12849 | autistic disorder | HGNC:14287 | Homo sapiens (human) | 57502 | NLGN4X |
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| DOID:0111662 | ectodermal dysplasia 14 | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:959 | Homo sapiens (human) | 581 | BAX |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:0112159 | autosomal dominant nonsyndromic deafness 78 | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0111795 | congenital nystagmus 6 | HGNC:20145 | Homo sapiens (human) | 4935 | GPR143 |
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| DOID:0050689 | brachydactyly-syndactyly syndrome | HGNC:5136 | Homo sapiens (human) | 3239 | HOXD13 |
|
