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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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MIRAGE
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:0080046 | Stickler syndrome | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:0111474 | combined oxidative phosphorylation deficiency 1 | HGNC:13780 | Homo sapiens (human) | 85476 | GFM1 |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:0080272 | nephrotic syndrome type 16 | HGNC:29300 | Homo sapiens (human) | 25959 | KANK2 |
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| DOID:5419 | schizophrenia | HGNC:4600 | Homo sapiens (human) | 2918 | GRM8 |
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| DOID:0080346 | blepharocheilodontic syndrome 2 | HGNC:2515 | Homo sapiens (human) | 1500 | CTNND1 |
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| DOID:4448 | macular degeneration | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:5980 | Homo sapiens (human) | 3603 | IL16 |
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| DOID:4247 | coronary restenosis | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:0080282 | developmental and epileptic encephalopathy 56 | HGNC:12852 | Homo sapiens (human) | 7532 | YWHAG |
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| DOID:0080977 | aortic valve disease 3 | HGNC:17985 | Homo sapiens (human) | 54538 | ROBO4 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:12849 | autistic disorder | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:2394 | ovarian cancer | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0110501 | autosomal recessive nonsyndromic deafness 44 | HGNC:232 | Homo sapiens (human) | 107 | ADCY1 |
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| DOID:707 | B-cell lymphoma | HGNC:74 | Homo sapiens (human) | 9429 | ABCG2 |
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| DOID:9256 | colorectal cancer | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:10003 | sensorineural hearing loss | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:2977 | primary hyperoxaluria | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:0070536 | neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0080978 | arthrogryposis multiplex congenita-1 | HGNC:18712 | Homo sapiens (human) | 163175 | LGI4 |
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| DOID:0050742 | nicotine dependence | HGNC:1958 | Homo sapiens (human) | 1137 | CHRNA4 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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