Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
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:0080046 | Stickler syndrome | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
|
||
| DOID:0070252 | autosomal dominant Emery-Dreifuss muscular dystrophy 7 | HGNC:28472 | Homo sapiens (human) | 79188 | TMEM43 |
|
||
| DOID:0080016 | spina bifida | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
|
||
| DOID:12148 | alveolar echinococcosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
|
||
| DOID:12010 | anterior ischemic optic neuropathy | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
|
||
| DOID:0111141 | delayed sleep phase syndrome | HGNC:2384 | Homo sapiens (human) | 1407 | CRY1 |
|
||
| DOID:0110592 | autosomal dominant nonsyndromic deafness 70 | HGNC:6944 | Homo sapiens (human) | 4171 | MCM2 |
|
||
| DOID:401 | multidrug-resistant tuberculosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
|
||
| DOID:0111019 | cone-rod dystrophy 12 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
|
||
| DOID:10003 | sensorineural hearing loss | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
|
||
| DOID:0081274 | peroxisome biogenesis disorder 14B | HGNC:8853 | Homo sapiens (human) | 8799 | PEX11B |
|
||
| DOID:2349 | arteriosclerosis | HGNC:7159 | Homo sapiens (human) | 4322 | MMP13 |
|
||
| DOID:0050748 | marginal zone lymphoma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
|
||
| DOID:0110589 | autosomal dominant nonsyndromic deafness 68 | HGNC:17513 | Homo sapiens (human) | 9455 | HOMER2 |
|
||
| DOID:9256 | colorectal cancer | HGNC:11896 | Homo sapiens (human) | 7128 | TNFAIP3 |
|
||
| DOID:0080285 | developmental and epileptic encephalopathy 58 | HGNC:8032 | Homo sapiens (human) | 4915 | NTRK2 |
|
||
| DOID:552 | pneumonia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
|
||
| DOID:2590 | familial nephrotic syndrome | HGNC:6485 | Homo sapiens (human) | 3911 | LAMA5 |
|
||
| DOID:12361 | Graves' disease | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
|
||
| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
|
||
| DOID:2377 | multiple sclerosis | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
|
||
| DOID:14448 | 46,XY sex reversal | HGNC:17210 | Homo sapiens (human) | 57647 | DHX37 |
|
||
| DOID:1245 | vulva cancer | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
|
||
| DOID:0050731 | vitamin B12 deficiency | HGNC:4013 | Homo sapiens (human) | 2524 | FUT2 |
|
||
| DOID:12241 | beta thalassemia | HGNC:4834 | Homo sapiens (human) | 10767 | HBS1L |
|
