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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:612 | primary immunodeficiency disease | HGNC:13178 | Homo sapiens (human) | 22806 | IKZF3 |
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| DOID:0080163 | otulipenia | HGNC:25118 | Homo sapiens (human) | 90268 | OTULIN |
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| DOID:0110484 | autosomal recessive nonsyndromic deafness 26 | HGNC:4066 | Homo sapiens (human) | 2549 | GAB1 |
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| DOID:0060889 | prune belly syndrome | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
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| DOID:0112352 | spermatogenic failure 58 | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:0070336 | arthrogryposis multiplex congenita-6 | HGNC:7720 | Homo sapiens (human) | 4703 | NEB |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:5006 | Homo sapiens (human) | 3156 | HMGCR |
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| DOID:12365 | malaria | HGNC:4035 | Homo sapiens (human) | 2532 | ACKR1 |
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| DOID:0080236 | autosomal dominant intellectual developmental disorder 45 | HGNC:14214 | Homo sapiens (human) | 23152 | CIC |
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| DOID:0050650 | familial atrial fibrillation | HGNC:777 | Homo sapiens (human) | 463 | ZFHX3 |
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| DOID:0111312 | idiopathic generalized epilepsy 11 | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:0111938 | immunodeficiency 24 | HGNC:2519 | Homo sapiens (human) | 1503 | CTPS1 |
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| DOID:0080770 | autosomal dominant beta thalassemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:0081002 | Cowden syndrome 6 | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:2565 | macular corneal dystrophy | HGNC:6938 | Homo sapiens (human) | 4166 | CHST6 |
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| DOID:0070165 | spermatogenic failure 18 | HGNC:2940 | Homo sapiens (human) | 25981 | DNAH1 |
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| DOID:0111954 | immunodeficiency 60 | HGNC:14078 | Homo sapiens (human) | 60468 | BACH2 |
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| DOID:0080297 | Coffin-Siris syndrome 6 | HGNC:18037 | Homo sapiens (human) | 196528 | ARID2 |
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| DOID:0080447 | developmental and epileptic encephalopathy 43 | HGNC:4083 | Homo sapiens (human) | 2562 | GABRB3 |
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| DOID:0112056 | X-linked intellectual disability-short stature-overweight syndrome | HGNC:19073 | Homo sapiens (human) | 57187 | THOC2 |
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| DOID:0070114 | Niemann-Pick disease type C2 | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
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| DOID:0111640 | autosomal recessive nonsyndromic deafness 111 | HGNC:3496 | Homo sapiens (human) | 10205 | MPZL2 |
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| DOID:0110652 | long QT syndrome 11 | HGNC:379 | Homo sapiens (human) | 10142 | AKAP9 |
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| DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:6647 | Homo sapiens (human) | 25802 | LMOD1 |
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| DOID:1793 | pancreatic cancer | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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