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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:0070529 | Sifrim-Hitz-Weiss syndrome | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
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| DOID:0070210 | hereditary lymphedema IA | HGNC:3767 | Homo sapiens (human) | 2324 | FLT4 |
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| DOID:0080289 | orofaciodigital syndrome XVII | HGNC:29239 | Homo sapiens (human) | 27152 | INTU |
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| DOID:0060706 | X-linked lymphoproliferative syndrome 2 | HGNC:592 | Homo sapiens (human) | 331 | XIAP |
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| DOID:0111584 | dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0111162 | epidermal nevus | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:6846 | familial melanoma | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0111019 | cone-rod dystrophy 12 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:0081147 | common variable immunodeficiency 4 | HGNC:17755 | Homo sapiens (human) | 115650 | TNFRSF13C |
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| DOID:612 | primary immunodeficiency disease | HGNC:17967 | Homo sapiens (human) | 51135 | IRAK4 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:13394 | Homo sapiens (human) | 7827 | NPHS2 |
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| DOID:0112181 | Schinzel type phocomelia | HGNC:12786 | Homo sapiens (human) | 7476 | WNT7A |
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| DOID:0070389 | developmental and epileptic encephalopathy 103 | HGNC:6234 | Homo sapiens (human) | 3747 | KCNC2 |
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| DOID:0081203 | autosomal recessive intellectual developmental disorder 38 | HGNC:4868 | Homo sapiens (human) | 8924 | HERC2 |
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| DOID:0110521 | autosomal recessive nonsyndromic deafness 70 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
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| DOID:5419 | schizophrenia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0081150 | common variable immunodeficiency 7 | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:0050974 | spinocerebellar ataxia type 25 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
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| DOID:0060765 | autosomal dominant Robinow syndrome 2 | HGNC:3084 | Homo sapiens (human) | 1855 | DVL1 |
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| DOID:0050545 | visceral heterotaxy | HGNC:7865 | Homo sapiens (human) | 4838 | NODAL |
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| DOID:0111608 | distal arthrogryposis type 5 | HGNC:26270 | Homo sapiens (human) | 63895 | PIEZO2 |
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| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
|
