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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
LM-GlycoRepo
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:0080696 | Winchester syndrome | HGNC:7160 | Homo sapiens (human) | 4323 | MMP14 |
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| DOID:10591 | pre-eclampsia | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:3459 | breast carcinoma | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0060870 | isolated growth hormone deficiency | HGNC:4263 | Homo sapiens (human) | 2690 | GHR |
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| DOID:10873 | Kuhnt-Junius degeneration | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:11054 | urinary bladder cancer | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0111847 | osteogenesis imperfecta type 19 | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:10608 | celiac disease | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:13884 | sick sinus syndrome | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:3312 | bipolar disorder | HGNC:896 | Homo sapiens (human) | 553 | AVPR1B |
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| DOID:0111769 | 46,XY sex reversal 6 | HGNC:6848 | Homo sapiens (human) | 4214 | MAP3K1 |
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| DOID:1324 | lung cancer | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:13042 | persistent fetal circulation syndrome | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:4257 | Caffey disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0111876 | linear skin defects with multiple congenital anomalies 3 | HGNC:20372 | Homo sapiens (human) | 54539 | NDUFB11 |
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| DOID:3910 | lung adenocarcinoma | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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| DOID:0070177 | spermatogenic failure 22 | HGNC:28569 | Homo sapiens (human) | 254528 | MEIOB |
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| DOID:399 | tuberculosis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:655 | inherited metabolic disorder | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:11294 | arteriovenous malformation | HGNC:3349 | Homo sapiens (human) | 2022 | ENG |
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| DOID:8552 | chronic myeloid leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:2770 | Homo sapiens (human) | 1674 | DES |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:11784 | Homo sapiens (human) | 7056 | THBD |
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| DOID:3883 | Lynch syndrome | HGNC:10050 | Homo sapiens (human) | 6041 | RNASEL |
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