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:0081350 | congenital myopathy 18 | HGNC:1397 | Homo sapiens (human) | 779 | CACNA1S |
|
||
| DOID:13241 | Behcet's disease | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
|
||
| DOID:0050742 | nicotine dependence | HGNC:5297 | Homo sapiens (human) | 3359 | HTR3A |
|
||
| DOID:9252 | amino acid metabolic disorder | HGNC:8923 | Homo sapiens (human) | 26227 | PHGDH |
|
||
| DOID:11162 | respiratory failure | HGNC:10801 | Homo sapiens (human) | 6439 | SFTPB |
|
||
| DOID:0111365 | benign familial hematuria | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:10952 | nephritis | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
|
||
| DOID:1923 | disorder of sexual development | HGNC:464 | Homo sapiens (human) | 268 | AMH |
|
||
| DOID:0080600 | COVID-19 | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
|
||
| DOID:3393 | coronary artery disease | HGNC:7978 | Homo sapiens (human) | 2908 | NR3C1 |
|
||
| DOID:9256 | colorectal cancer | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
|
||
| DOID:0080046 | Stickler syndrome | HGNC:2219 | Homo sapiens (human) | 1299 | COL9A3 |
|
||
| DOID:0060374 | orofaciodigital syndrome IV | HGNC:24519 | Homo sapiens (human) | 26123 | TCTN3 |
|
||
| DOID:0070517 | retinal macular dystrophy 2 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
|
||
| DOID:9952 | acute lymphoblastic leukemia | HGNC:2348 | Homo sapiens (human) | 1387 | CREBBP |
|
||
| DOID:2841 | asthma | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
|
||
| DOID:0080028 | spondyloepimetaphyseal dysplasia, Strudwick type | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
|
||
| DOID:2513 | basal cell carcinoma | HGNC:15762 | Homo sapiens (human) | 51340 | CRNKL1 |
|
||
| DOID:0050860 | colorectal adenoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
|
||
| DOID:10763 | hypertension | HGNC:79 | Homo sapiens (human) | 28 | ABO |
|
||
| DOID:1094 | attention deficit hyperactivity disorder | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
|
||
| DOID:0111334 | congenital leptin deficiency | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
|
||
| DOID:0111682 | diffuse cystic renal dysplasia | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
|
||
| DOID:0112332 | pontocerebellar hypoplasia type 13 | HGNC:1172 | Homo sapiens (human) | 738 | VPS51 |
|
||
| DOID:2218 | blood platelet disease | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
|
