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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:0070425 | combined oxidative phosphorylation deficiency 52 | HGNC:15910 | Homo sapiens (human) | 9054 | NFS1 |
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| DOID:14415 | Legg-Calve-Perthes disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0081164 | dilated cardiomyopathy 3B | HGNC:2928 | Homo sapiens (human) | 1756 | DMD |
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| DOID:0080090 | reducing body myopathy 1A | HGNC:3702 | Homo sapiens (human) | 2273 | FHL1 |
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| DOID:0110542 | autosomal dominant nonsyndromic deafness 10 | HGNC:3522 | Homo sapiens (human) | 2070 | EYA4 |
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| DOID:0060241 | 3-M syndrome | HGNC:29092 | Homo sapiens (human) | 23363 | OBSL1 |
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| DOID:0050984 | spinocerebellar ataxia type 37 | HGNC:2661 | Homo sapiens (human) | 1600 | DAB1 |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:9958 | Homo sapiens (human) | 5972 | REN |
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| DOID:0111941 | immunodeficiency 20 | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0070013 | Seckel syndrome 2 | HGNC:9891 | Homo sapiens (human) | 5932 | RBBP8 |
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| DOID:0111010 | cone-rod dystrophy 5 | HGNC:21043 | Homo sapiens (human) | 83394 | PITPNM3 |
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| DOID:0070376 | developmental and epileptic encephalopathy 31B | HGNC:2972 | Homo sapiens (human) | 1759 | DNM1 |
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| DOID:0110461 | X-linked dilated cardiomyopathy | HGNC:2928 | Homo sapiens (human) | 1756 | DMD |
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| DOID:0081123 | X-linked mental retardation Gustavson type | HGNC:9910 | Homo sapiens (human) | 27316 | RBMX |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:0112303 | spondylometaphyseal dysplasia with corneal dystrophy | HGNC:9056 | Homo sapiens (human) | 5331 | PLCB3 |
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| DOID:2513 | basal cell carcinoma | HGNC:9586 | Homo sapiens (human) | 8643 | PTCH2 |
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| DOID:0080975 | intracranial berry aneurysm 12 | HGNC:17754 | Homo sapiens (human) | 55901 | THSD1 |
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| DOID:0112166 | autosomal dominant nonsyndromic deafness 75 | HGNC:12347 | Homo sapiens (human) | 8295 | TRRAP |
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| DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:0112338 | spermatogenic failure 57 | HGNC:21185 | Homo sapiens (human) | 154197 | PNLDC1 |
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| DOID:12849 | autistic disorder | HGNC:26392 | Homo sapiens (human) | 139411 | PTCHD1 |
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| DOID:0112108 | myofibrillar myopathy 10 | HGNC:11480 | Homo sapiens (human) | 6840 | SVIL |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:16404 | Homo sapiens (human) | 112744 | IL17F |
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| DOID:0080281 | schizophrenia 19 | HGNC:9898 | Homo sapiens (human) | 10137 | RBM12 |
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