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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:0112243 | congenital symmetric circumferential skin creases 2 | HGNC:6891 | Homo sapiens (human) | 10982 | MAPRE2 |
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| DOID:4051 | alveolar rhabdomyosarcoma | HGNC:3819 | Homo sapiens (human) | 2308 | FOXO1 |
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| DOID:0081224 | autosomal recessive intellectual developmental disorder 63 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0112348 | hereditary spastic paraplegia 78 | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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| DOID:0080632 | Fazio-Londe disease | HGNC:16187 | Homo sapiens (human) | 113278 | SLC52A3 |
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| DOID:0111286 | psoriasis 1 | HGNC:4933 | Homo sapiens (human) | 3107 | HLA-C |
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| DOID:0111108 | maturity-onset diabetes of the young type 10 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:0080625 | severe congenital neutropenia 1 | HGNC:3309 | Homo sapiens (human) | 1991 | ELANE |
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| DOID:0050465 | Muir-Torre syndrome | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0111821 | ichthyosis follicularis-alopecia-photophobia syndrome 1 | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:6189 | Homo sapiens (human) | 3714 | JAG2 |
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| DOID:0112361 | spondylocostal dysostosis 3 | HGNC:6560 | Homo sapiens (human) | 3955 | LFNG |
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| DOID:10123 | pigmentation disease | HGNC:6343 | Homo sapiens (human) | 4254 | KITLG |
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| DOID:0070370 | restrictive dermopathy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0081339 | congenital myopathy 2B | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:20758 | Homo sapiens (human) | 84936 | ZFYVE19 |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:9052 | Homo sapiens (human) | 5328 | PLAU |
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| DOID:0110587 | autosomal dominant nonsyndromic deafness 66 | HGNC:1632 | Homo sapiens (human) | 8763 | CD164 |
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| DOID:0080981 | arthrogryposis multiplex congenita-5 | HGNC:3098 | Homo sapiens (human) | 1861 | TOR1A |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:28526 | Homo sapiens (human) | 285203 | EOGT |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:5035 | Homo sapiens (human) | 3183 | HNRNPC |
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| DOID:0111959 | immunodeficiency 15B | HGNC:5960 | Homo sapiens (human) | 3551 | IKBKB |
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| DOID:0081235 | autosomal recessive intellectual developmental disorder 76 | HGNC:4571 | Homo sapiens (human) | 2890 | GRIA1 |
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