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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:784 | chronic kidney disease | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:0070376 | developmental and epileptic encephalopathy 31B | HGNC:2972 | Homo sapiens (human) | 1759 | DNM1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:8893 | psoriasis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:5419 | schizophrenia | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:6693 | Homo sapiens (human) | 53353 | LRP1B |
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| DOID:10941 | intracranial aneurysm | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0050784 | primary progressive multiple sclerosis | HGNC:14899 | Homo sapiens (human) | 140766 | ADAMTS14 |
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| DOID:0110461 | X-linked dilated cardiomyopathy | HGNC:2928 | Homo sapiens (human) | 1756 | DMD |
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| DOID:594 | panic disorder | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0081123 | X-linked mental retardation Gustavson type | HGNC:9910 | Homo sapiens (human) | 27316 | RBMX |
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| DOID:0060305 | megalocornea | HGNC:6715 | Homo sapiens (human) | 4053 | LTBP2 |
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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:10591 | pre-eclampsia | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:3068 | glioblastoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0112303 | spondylometaphyseal dysplasia with corneal dystrophy | HGNC:9056 | Homo sapiens (human) | 5331 | PLCB3 |
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| DOID:0060041 | autism spectrum disorder | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:10763 | hypertension | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:2513 | basal cell carcinoma | HGNC:9586 | Homo sapiens (human) | 8643 | PTCH2 |
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| DOID:1168 | familial hyperlipidemia | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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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:9352 | type 2 diabetes mellitus | HGNC:8744 | Homo sapiens (human) | 5126 | PCSK2 |
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| DOID:9976 | heroin dependence | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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