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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
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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:0111076 | progressive familial heart block type IB | HGNC:17993 | Homo sapiens (human) | 54795 | TRPM4 |
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| DOID:417 | autoimmune disease | HGNC:18187 | Homo sapiens (human) | 54414 | SIAE |
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| DOID:0070217 | familial hyperinsulinemic hypoglycemia 6 | HGNC:4335 | Homo sapiens (human) | 2746 | GLUD1 |
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| DOID:0080792 | Treacher Collins syndrome 4 | HGNC:20454 | Homo sapiens (human) | 84172 | POLR1B |
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| DOID:0110221 | Brugada syndrome 4 | HGNC:1402 | Homo sapiens (human) | 783 | CACNB2 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:9119 | acute myeloid leukemia | HGNC:6342 | Homo sapiens (human) | 3815 | KIT |
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| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0111404 | Jalili syndrome | HGNC:105 | Homo sapiens (human) | 26504 | CNNM4 |
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| DOID:0110807 | hereditary spastic paraplegia 55 | HGNC:26784 | Homo sapiens (human) | 91574 | MTRFR |
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| DOID:0111996 | immunodeficiency 51 | HGNC:5985 | Homo sapiens (human) | 23765 | IL17RA |
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| DOID:0110584 | autosomal dominant nonsyndromic deafness 6 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:2841 | asthma | HGNC:7518 | Homo sapiens (human) | 4589 | MUC7 |
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| DOID:0112223 | developmental and epileptic encephalopathy 89 | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0111919 | spermatogenic failure 38 | HGNC:23045 | Homo sapiens (human) | 84071 | ARMC2 |
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| DOID:0060898 | Parkinson's disease 20 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0112129 | severe congenital neutropenia 7 | HGNC:2439 | Homo sapiens (human) | 1441 | CSF3R |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:20844 | Homo sapiens (human) | 165829 | GPR156 |
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| DOID:0111322 | idiopathic generalized epilepsy 8 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0070287 | primary autosomal recessive microcephaly 11 | HGNC:3182 | Homo sapiens (human) | 1911 | PHC1 |
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| DOID:0060549 | Barber-Say syndrome | HGNC:20670 | Homo sapiens (human) | 117581 | TWIST2 |
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| DOID:0080020 | Jansen's metaphyseal chondrodysplasia | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:0050578 | occult macular dystrophy | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:29216 | Homo sapiens (human) | 57514 | ARHGAP31 |
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