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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:11044 | gastroschisis | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:0112152 | CHIME syndrome | HGNC:8966 | Homo sapiens (human) | 9487 | PIGL |
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| DOID:0080526 | bronchiectasis 1 | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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| DOID:820 | myocarditis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0080523 | adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | HGNC:2433 | Homo sapiens (human) | 1436 | CSF1R |
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| DOID:811 | lipodystrophy | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:12449 | aplastic anemia | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:1558 | angioedema | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
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| DOID:5419 | schizophrenia | HGNC:6700 | Homo sapiens (human) | 7804 | LRP8 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:3070 | high grade glioma | HGNC:9393 | Homo sapiens (human) | 5578 | PRKCA |
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| DOID:14748 | Sotos syndrome | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:8704 | genital herpes | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:0081146 | common variable immunodeficiency 3 | HGNC:1633 | Homo sapiens (human) | 930 | CD19 |
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| DOID:11335 | sarcoidosis | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:0070130 | autosomal dominant cutis laxa 1 | HGNC:3327 | Homo sapiens (human) | 2006 | ELN |
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| DOID:0081177 | autosomal recessive intellectual developmental disorder 1 | HGNC:9477 | Homo sapiens (human) | 8492 | PRSS12 |
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| DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:0111428 | essential tremor 1 | HGNC:3024 | Homo sapiens (human) | 1814 | DRD3 |
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| DOID:4959 | epidermolysis bullosa dystrophica | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:3565 | meningioma | HGNC:11103 | Homo sapiens (human) | 6598 | SMARCB1 |
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| DOID:3393 | coronary artery disease | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:8886 | chorioretinitis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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