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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:0050866 | oral squamous cell carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:2957 | pulmonary tuberculosis | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:12030 | panuveitis | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:784 | chronic kidney disease | HGNC:6357 | Homo sapiens (human) | 3816 | KLK1 |
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| DOID:0111111 | maturity-onset diabetes of the young type 14 | HGNC:24035 | Homo sapiens (human) | 26060 | APPL1 |
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| DOID:3883 | Lynch syndrome | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:10825 | essential hypertension | HGNC:3146 | Homo sapiens (human) | 1889 | ECE1 |
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| DOID:10763 | hypertension | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0080675 | Stickler syndrome 2 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0111365 | benign familial hematuria | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
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| DOID:9884 | muscular dystrophy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:9775 | diastolic heart failure | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:0060883 | intestinal hypomagnesemia 1 | HGNC:17995 | Homo sapiens (human) | 140803 | TRPM6 |
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| DOID:0080551 | Naxos disease | HGNC:6207 | Homo sapiens (human) | 3728 | JUP |
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| DOID:14744 | Partington syndrome | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:2596 | larynx cancer | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:0060224 | atrial fibrillation | HGNC:6240 | Homo sapiens (human) | 3753 | KCNE1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:7097 | Homo sapiens (human) | 4282 | MIF |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:10763 | hypertension | HGNC:3020 | Homo sapiens (human) | 1812 | DRD1 |
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| DOID:13399 | color blindness | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:11713 | diabetic angiopathy | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:0110984 | Joubert syndrome 15 | HGNC:12370 | Homo sapiens (human) | 95681 | CEP41 |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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