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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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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:14330 | Parkinson's disease | HGNC:30511 | Homo sapiens (human) | 90522 | YIF1B |
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| DOID:0070425 | combined oxidative phosphorylation deficiency 52 | HGNC:15910 | Homo sapiens (human) | 9054 | NFS1 |
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| DOID:0060439 | lysinuric protein intolerance | HGNC:11065 | Homo sapiens (human) | 9056 | SLC7A7 |
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| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
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| DOID:14447 | gonadal dysgenesis | HGNC:19164 | Homo sapiens (human) | 90627 | STARD13 |
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| DOID:2531 | hematologic cancer | HGNC:17311 | Homo sapiens (human) | 9063 | PIAS2 |
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| DOID:670 | amphetamine abuse | HGNC:6858 | Homo sapiens (human) | 9064 | MAP3K6 |
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| DOID:0050155 | sensory system disease | HGNC:18502 | Homo sapiens (human) | 90665 | TBL1Y |
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| DOID:0111758 | Y-linked deafness 2 | HGNC:18502 | Homo sapiens (human) | 90665 | TBL1Y |
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| DOID:0110169 | Charcot-Marie-Tooth disease axonal type 2P | HGNC:25135 | Homo sapiens (human) | 90678 | LRSAM1 |
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| DOID:5419 | schizophrenia | HGNC:744 | Homo sapiens (human) | 9070 | ASH2L |
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| DOID:9778 | irritable bowel syndrome | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:5082 | liver cirrhosis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:3310 | atopic dermatitis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:824 | periodontitis | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:8778 | Crohn's disease | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:687 | hepatoblastoma | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:8947 | diabetic retinopathy | HGNC:2032 | Homo sapiens (human) | 9076 | CLDN1 |
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| DOID:10273 | heart conduction disease | HGNC:30257 | Homo sapiens (human) | 90780 | PYGO2 |
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| DOID:0060036 | intrinsic cardiomyopathy | HGNC:1620 | Homo sapiens (human) | 908 | CCT6A |
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| DOID:0112162 | autosomal recessive nonsyndromic deafness 116 | HGNC:2051 | Homo sapiens (human) | 9080 | CLDN9 |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:649 | prion disease | HGNC:12612 | Homo sapiens (human) | 9097 | USP14 |
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