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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:5844 | myocardial infarction | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:0110839 | Usher syndrome type 2C | RGD:621208 | Rattus norvegicus (Norway rat) | 117955 | Slc4a7 |
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| DOID:2355 | anemia | RGD:621208 | Rattus norvegicus (Norway rat) | 117955 | Slc4a7 |
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| DOID:0111222 | centronuclear myopathy 5 | MGI:109282 | Mus musculus (house mouse) | 11790 | Speg |
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| DOID:1485 | cystic fibrosis | HGNC:2015 | Homo sapiens (human) | 1179 | CLCA1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2015 | Homo sapiens (human) | 1179 | CLCA1 |
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| DOID:2841 | asthma | HGNC:2015 | Homo sapiens (human) | 1179 | CLCA1 |
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| DOID:10652 | Alzheimer's disease | MGI:107765 | Mus musculus (house mouse) | 11785 | Apbb1 |
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| DOID:0080448 | developmental and epileptic encephalopathy 48 | MGI:1100869 | Mus musculus (house mouse) | 11775 | Ap3b2 |
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| DOID:1227 | neutropenia | MGI:1333879 | Mus musculus (house mouse) | 11774 | Ap3b1 |
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| DOID:3753 | Hermansky-Pudlak syndrome | MGI:1333879 | Mus musculus (house mouse) | 11774 | Ap3b1 |
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| DOID:3770 | pulmonary fibrosis | MGI:1333879 | Mus musculus (house mouse) | 11774 | Ap3b1 |
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| DOID:0060540 | Hermansky-Pudlak syndrome 2 | MGI:1333879 | Mus musculus (house mouse) | 11774 | Ap3b1 |
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| DOID:3082 | interstitial lung disease | MGI:1333879 | Mus musculus (house mouse) | 11774 | Ap3b1 |
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| DOID:2223 | platelet storage pool deficiency | MGI:1333879 | Mus musculus (house mouse) | 11774 | Ap3b1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | MGI:1298405 | Mus musculus (house mouse) | 11773 | Ap2m1 |
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| DOID:3969 | thyroid gland papillary carcinoma | MGI:2152936 | Mus musculus (house mouse) | 117600 | Srgap1 |
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| DOID:1312 | focal segmental glomerulosclerosis | MGI:2152936 | Mus musculus (house mouse) | 117600 | Srgap1 |
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| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | MGI:2152819 | Mus musculus (house mouse) | 117592 | B3galt6 |
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| DOID:13359 | Ehlers-Danlos syndrome | MGI:2152819 | Mus musculus (house mouse) | 117592 | B3galt6 |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | MGI:2152819 | Mus musculus (house mouse) | 117592 | B3galt6 |
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| DOID:0060611 | abdominal obesity-metabolic syndrome | MGI:2152844 | Mus musculus (house mouse) | 117591 | Slc2a9 |
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| DOID:1920 | hyperuricemia | MGI:2152844 | Mus musculus (house mouse) | 117591 | Slc2a9 |
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| DOID:0060549 | Barber-Say syndrome | HGNC:20670 | Homo sapiens (human) | 117581 | TWIST2 |
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| DOID:14768 | Saethre-Chotzen syndrome | HGNC:20670 | Homo sapiens (human) | 117581 | TWIST2 |
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