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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:1324 | lung cancer | HGNC:3527 | Homo sapiens (human) | 2146 | EZH2 |
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| DOID:2841 | asthma | HGNC:4964 | Homo sapiens (human) | 3135 | HLA-G |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:76 | Homo sapiens (human) | 25 | ABL1 |
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| DOID:3393 | coronary artery disease | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:2043 | hepatitis B | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:7608 | Homo sapiens (human) | 4649 | MYO9A |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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| DOID:4997 | Camurati-Engelmann disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0080431 | developmental and epileptic encephalopathy 19 | HGNC:4075 | Homo sapiens (human) | 2554 | GABRA1 |
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| DOID:1184 | nephrotic syndrome | RGD:3640 | Rattus norvegicus (Norway rat) | 24767 | Scnn1b |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:0081116 | benign familial infantile seizures 3 | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:9976 | heroin dependence | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0110064 | amelogenesis imperfecta type 1H | HGNC:6161 | Homo sapiens (human) | 3694 | ITGB6 |
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| DOID:381 | arthropathy | HGNC:12771 | Homo sapiens (human) | 8838 | CCN6 |
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| DOID:7147 | ankylosing spondylitis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0070288 | primary autosomal recessive microcephaly 17 | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:0060213 | frontotemporal dementia and/or amyotrophic lateral sclerosis 1 | HGNC:28337 | Homo sapiens (human) | 203228 | C9orf72 |
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| DOID:9993 | hypoglycemia | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:9452 | steatotic liver disease | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0050591 | tooth agenesis | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0081333 | Wiedemann-Rautenstrauch syndrome | HGNC:30074 | Homo sapiens (human) | 11128 | POLR3A |
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| DOID:0060302 | type II complement component 8 deficiency | HGNC:1353 | Homo sapiens (human) | 732 | C8B |
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