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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:0050789 | tarsal-carpal coalition syndrome | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:10534 | stomach cancer | HGNC:13726 | Homo sapiens (human) | 58508 | KMT2C |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0060654 | lethal congenital contracture syndrome 4 | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1959 | Homo sapiens (human) | 1138 | CHRNA5 |
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| DOID:12849 | autistic disorder | HGNC:6297 | Homo sapiens (human) | 3786 | KCNQ3 |
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| DOID:552 | pneumonia | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0081119 | benign familial infantile seizures 6 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:0111953 | immunodeficiency 23 | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:10283 | prostate cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:13241 | Behcet's disease | HGNC:6014 | Homo sapiens (human) | 3565 | IL4 |
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| DOID:0111313 | idiopathic generalized epilepsy 12 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0050975 | spinocerebellar ataxia type 26 | HGNC:3214 | Homo sapiens (human) | 1938 | EEF2 |
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| DOID:0060258 | reticulate acropigmentation of Kitamura | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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| DOID:0050117 | disease by infectious agent | HGNC:3437 | Homo sapiens (human) | 2073 | ERCC5 |
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| DOID:2527 | nephrosis | HGNC:4172 | Homo sapiens (human) | 2625 | GATA3 |
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| DOID:8866 | actinic keratosis | HGNC:8101 | Homo sapiens (human) | 4948 | OCA2 |
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| DOID:3996 | urinary system cancer | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:0070004 | myeloid neoplasm | HGNC:1541 | Homo sapiens (human) | 867 | CBL |
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| DOID:1380 | endometrial cancer | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0112098 | nuclear type mitochondrial complex I deficiency 30 | HGNC:20372 | Homo sapiens (human) | 54539 | NDUFB11 |
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| DOID:2860 | hemoglobinopathy | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:9119 | acute myeloid leukemia | HGNC:6679 | Homo sapiens (human) | 4026 | LPP |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:0080579 | 3-Methylcrotonyl-CoA carboxylase 1 deficiency | HGNC:6936 | Homo sapiens (human) | 56922 | MCCC1 |
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