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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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MIRAGE
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:0111425 | restrictive cardiomyopathy 1 | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:0111740 | X-linked deafness 6 | HGNC:2208 | Homo sapiens (human) | 1288 | COL4A6 |
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| DOID:0110965 | brachydactyly type A2 | HGNC:1069 | Homo sapiens (human) | 650 | BMP2 |
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| DOID:0081190 | autosomal recessive intellectual developmental disorder 18 | HGNC:2372 | Homo sapiens (human) | 9439 | MED23 |
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| DOID:0110444 | dilated cardiomyopathy 1X | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:612 | primary immunodeficiency disease | HGNC:15632 | Homo sapiens (human) | 51311 | TLR8 |
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| DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:0081212 | autosomal recessive intellectual developmental disorder 48 | HGNC:31399 | Homo sapiens (human) | 388662 | SLC6A17 |
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| DOID:0070454 | hereditary spastic paraplegia 70 | HGNC:6898 | Homo sapiens (human) | 4141 | MARS1 |
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| DOID:0110026 | age related macular degeneration 14 | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0081344 | congenital myopathy 9B | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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| DOID:0060746 | basal laminar drusen | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:0081226 | autosomal recessive intellectual developmental disorder 65 | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:9410 | panhypopituitarism | HGNC:10249 | Homo sapiens (human) | 6091 | ROBO1 |
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| DOID:0112187 | thyroid dyshormonogenesis 3 | HGNC:11764 | Homo sapiens (human) | 7038 | TG |
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| DOID:0080688 | mosaic variegated aneuploidy syndrome | HGNC:17814 | Homo sapiens (human) | 55719 | SLF2 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:10830 | Homo sapiens (human) | 6455 | SH3GL1 |
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| DOID:0060668 | anencephaly | HGNC:29558 | Homo sapiens (human) | 81788 | NUAK2 |
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| DOID:0050646 | distal arthrogryposis | HGNC:16305 | Homo sapiens (human) | 170689 | ADAMTS15 |
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| DOID:0110013 | advanced sleep phase syndrome 3 | HGNC:8847 | Homo sapiens (human) | 8863 | PER3 |
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| DOID:4253 | melorheostosis | HGNC:6840 | Homo sapiens (human) | 5604 | MAP2K1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6882 | Homo sapiens (human) | 9479 | MAPK8IP1 |
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