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:1115 | sarcoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
|
||
| DOID:0070538 | syndromic X-linked intellectual developmental disorder bain type | HGNC:5042 | Homo sapiens (human) | 3188 | HNRNPH2 |
|
||
| DOID:9074 | systemic lupus erythematosus | HGNC:3618 | Homo sapiens (human) | 2213 | FCGR2B |
|
||
| DOID:1388 | Tangier disease | HGNC:29 | Homo sapiens (human) | 19 | ABCA1 |
|
||
| DOID:8398 | osteoarthritis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
|
||
| DOID:14768 | Saethre-Chotzen syndrome | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
|
||
| DOID:0111002 | Joubert syndrome 7 | HGNC:29168 | Homo sapiens (human) | 23322 | RPGRIP1L |
|
||
| DOID:0111789 | Frank-Ter Haar syndrome | HGNC:29242 | Homo sapiens (human) | 285590 | SH3PXD2B |
|
||
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
|
||
| DOID:2746 | glycogen storage disease V | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
|
||
| DOID:0050659 | biotin-responsive basal ganglia disease | HGNC:16266 | Homo sapiens (human) | 80704 | SLC19A3 |
|
||
| DOID:0050560 | Walker-Warburg syndrome | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
|
||
| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
|
||
| DOID:0111042 | glycogen storage disease IXa | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
|
||
| DOID:0111113 | nephronophthisis 2 | HGNC:17870 | Homo sapiens (human) | 27130 | INVS |
|
||
| DOID:0050589 | inflammatory bowel disease | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
|
||
| DOID:0111464 | combined oxidative phosphorylation deficiency 35 | HGNC:20286 | Homo sapiens (human) | 54802 | TRIT1 |
|
||
| DOID:0060684 | autosomal dominant nocturnal frontal lobe epilepsy 3 | HGNC:1962 | Homo sapiens (human) | 1141 | CHRNB2 |
|
||
| DOID:0050547 | familial medullary thyroid carcinoma | HGNC:9967 | Homo sapiens (human) | 5979 | RET |
|
||
| DOID:0081060 | X-linked nephrogenic diabetes insipidus | HGNC:897 | Homo sapiens (human) | 554 | AVPR2 |
|
||
| DOID:0111041 | glycogen storage disease IXb | HGNC:8927 | Homo sapiens (human) | 5257 | PHKB |
|
||
| DOID:0111459 | classic galactosemia | HGNC:4135 | Homo sapiens (human) | 2592 | GALT |
|
||
| DOID:3526 | cerebral infarction | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
|
||
| DOID:0050475 | Weill-Marchesani syndrome | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
|
