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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:0080807 | autosomal dominant craniodiaphyseal dysplasia | HGNC:13771 | Homo sapiens (human) | 50964 | SOST |
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| DOID:0070120 | Meckel syndrome 6 | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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| DOID:1474 | aggressive periodontitis | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:0110825 | hereditary spastic paraplegia 9B | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0050462 | Antley-Bixler syndrome with disordered steroidogenesis | HGNC:9208 | Homo sapiens (human) | 5447 | POR |
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| DOID:0081344 | congenital myopathy 9B | HGNC:4023 | Homo sapiens (human) | 8087 | FXR1 |
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| DOID:0110438 | dilated cardiomyopathy 1JJ | HGNC:6484 | Homo sapiens (human) | 3910 | LAMA4 |
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| DOID:0110288 | autosomal recessive limb-girdle muscular dystrophy type 2W | HGNC:16084 | Homo sapiens (human) | 55679 | LIMS2 |
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| DOID:0112336 | spermatogenic failure 56 | HGNC:2941 | Homo sapiens (human) | 196385 | DNAH10 |
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| DOID:12842 | Guillain-Barre syndrome | HGNC:9118 | Homo sapiens (human) | 5376 | PMP22 |
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| DOID:0111741 | X-linked deafness 5 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:2121 | ectodermal dysplasia | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:0111972 | immunodeficiency 19 | HGNC:1673 | Homo sapiens (human) | 915 | CD3D |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:2484 | Homo sapiens (human) | 1478 | CSTF2 |
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| DOID:0111260 | phosphoribosylpyrophosphate synthetase superactivity | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0070033 | autosomal dominant intellectual developmental disorder 3 | HGNC:1754 | Homo sapiens (human) | 1013 | CDH15 |
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| DOID:0081337 | congenital myopathy | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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| DOID:0080232 | autosomal dominant intellectual developmental disorder 51 | HGNC:24283 | Homo sapiens (human) | 51111 | KMT5B |
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| DOID:0080076 | Neu-Laxova syndrome 1 | HGNC:8923 | Homo sapiens (human) | 26227 | PHGDH |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:1014 | Homo sapiens (human) | 613 | BCR |
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| DOID:0070182 | spermatogenic failure 13 | HGNC:11538 | Homo sapiens (human) | 6875 | TAF4B |
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| DOID:0112337 | spermatogenic failure 55 | HGNC:26620 | Homo sapiens (human) | 200162 | SPAG17 |
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| DOID:0080443 | developmental and epileptic encephalopathy 21 | HGNC:24539 | Homo sapiens (human) | 25977 | NECAP1 |
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| DOID:14283 | primary hypertrophic osteoarthropathy | HGNC:10955 | Homo sapiens (human) | 6578 | SLCO2A1 |
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