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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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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:0110770 | hereditary spastic paraplegia 17 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:0080420 | developmental and epileptic encephalopathy 62 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0112353 | spermatogenic failure 64 | HGNC:28521 | Homo sapiens (human) | 286151 | FBXO43 |
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| DOID:0112145 | retinitis pigmentosa 88 | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:0060387 | chondrodysplasia Blomstrand type | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:0060386 | Chilblain lupus | HGNC:15925 | Homo sapiens (human) | 25939 | SAMHD1 |
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| DOID:0060767 | autosomal dominant Robinow syndrome 3 | HGNC:3087 | Homo sapiens (human) | 1857 | DVL3 |
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| DOID:0080460 | developmental and epileptic encephalopathy 34 | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
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| DOID:0081378 | amyotrophic lateral sclerosis type 24 | HGNC:7744 | Homo sapiens (human) | 4750 | NEK1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:23357 | Homo sapiens (human) | 28985 | MCTS1 |
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| DOID:2218 | blood platelet disease | HGNC:3749 | Homo sapiens (human) | 2313 | FLI1 |
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| DOID:1172 | hyperlipoproteinemia type IV | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:18021 | Homo sapiens (human) | 11322 | TMC6 |
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| DOID:0111969 | immunodeficiency 39 | HGNC:6122 | Homo sapiens (human) | 3665 | IRF7 |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:26504 | Homo sapiens (human) | 123624 | AGBL1 |
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| DOID:0110857 | posterior polymorphous corneal dystrophy 3 | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:0080046 | Stickler syndrome | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:0070252 | autosomal dominant Emery-Dreifuss muscular dystrophy 7 | HGNC:28472 | Homo sapiens (human) | 79188 | TMEM43 |
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| DOID:0111141 | delayed sleep phase syndrome | HGNC:2384 | Homo sapiens (human) | 1407 | CRY1 |
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| DOID:0110592 | autosomal dominant nonsyndromic deafness 70 | HGNC:6944 | Homo sapiens (human) | 4171 | MCM2 |
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| DOID:0111019 | cone-rod dystrophy 12 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:0081274 | peroxisome biogenesis disorder 14B | HGNC:8853 | Homo sapiens (human) | 8799 | PEX11B |
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| DOID:0110589 | autosomal dominant nonsyndromic deafness 68 | HGNC:17513 | Homo sapiens (human) | 9455 | HOMER2 |
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| DOID:0080285 | developmental and epileptic encephalopathy 58 | HGNC:8032 | Homo sapiens (human) | 4915 | NTRK2 |
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