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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
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:6543 | acne | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0081401 | autosomal dominant distal hereditary motor neuronopathy 13 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:0070150 | hereditary sensory and autonomic neuropathy type 2B | HGNC:25964 | Homo sapiens (human) | 54463 | RETREG1 |
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| DOID:585 | nephrolithiasis | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:9383 | iridocyclitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0050864 | non-arteritic anterior ischemic optic neuropathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:14711 | FG syndrome | HGNC:11957 | Homo sapiens (human) | 9968 | MED12 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:2841 | asthma | HGNC:7590 | Homo sapiens (human) | 4638 | MYLK |
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| DOID:0110664 | congenital myasthenic syndrome 3C | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
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| DOID:0080960 | amelogenesis imperfecta type 2A6 | HGNC:4519 | Homo sapiens (human) | 8111 | GPR68 |
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| DOID:1099 | alpha thalassemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:2559 | opiate dependence | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:2349 | arteriosclerosis | HGNC:5141 | Homo sapiens (human) | 3240 | HP |
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| DOID:0112106 | chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
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| DOID:1270 | hereditary hemorrhagic telangiectasia | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:11613 | hyperandrogenism | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:3526 | cerebral infarction | HGNC:6145 | Homo sapiens (human) | 3680 | ITGA9 |
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| DOID:0111268 | autosomal recessive hyaline body myopathy | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:0050576 | Senior-Loken syndrome | HGNC:17861 | Homo sapiens (human) | 26146 | TRAF3IP1 |
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| DOID:6364 | migraine | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:9119 | acute myeloid leukemia | HGNC:16063 | Homo sapiens (human) | 8028 | MLLT10 |
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