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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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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:8158 | complement component 5 deficiency | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:10123 | pigmentation disease | HGNC:16472 | Homo sapiens (human) | 51151 | SLC45A2 |
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| DOID:0111988 | immunodeficiency 12 | HGNC:6819 | Homo sapiens (human) | 10892 | MALT1 |
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| DOID:0112209 | developmental and epileptic encephalopathy 73 | HGNC:10057 | Homo sapiens (human) | 11342 | RNF13 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0080866 | primary ovarian insufficiency 9 | HGNC:20193 | Homo sapiens (human) | 164045 | HFM1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6882 | Homo sapiens (human) | 9479 | MAPK8IP1 |
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| DOID:2154 | nephroblastoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | HGNC:9282 | Homo sapiens (human) | 5500 | PPP1CB |
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| DOID:0080346 | blepharocheilodontic syndrome 2 | HGNC:2515 | Homo sapiens (human) | 1500 | CTNND1 |
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| DOID:0060366 | Hennekam syndrome | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:0081320 | multiple synostoses syndrome 4 | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
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| DOID:0060448 | Fleck corneal dystrophy | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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| DOID:0060715 | autosomal recessive congenital ichthyosis 6 | HGNC:28018 | Homo sapiens (human) | 348938 | NIPAL4 |
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| DOID:0060395 | chromosome 15q24 deletion syndrome | HGNC:19353 | Homo sapiens (human) | 25942 | SIN3A |
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| DOID:0111638 | autosomal recessive nonsyndromic deafness 100 | HGNC:29035 | Homo sapiens (human) | 23262 | PPIP5K2 |
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| DOID:0110321 | hypertrophic cardiomyopathy 15 | HGNC:12665 | Homo sapiens (human) | 7414 | VCL |
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| DOID:0111647 | Schopf-Schulz-Passarge syndrome | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:0070291 | primary autosomal recessive microcephaly 4 | HGNC:24054 | Homo sapiens (human) | 57082 | KNL1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0111896 | Diamond-Blackfan anemia 18 | HGNC:10310 | Homo sapiens (human) | 6141 | RPL18 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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| DOID:0080672 | fibrochondrogenesis 1 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0080404 | orofacial cleft 11 | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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