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:12117 | pulmonary alveolar microlithiasis | HGNC:11020 | Homo sapiens (human) | 10568 | SLC34A2 |
|
||
| DOID:0111458 | galactose epimerase deficiency | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
|
||
| DOID:0111549 | aplasia of lacrimal and salivary glands | HGNC:3666 | Homo sapiens (human) | 2255 | FGF10 |
|
||
| DOID:0080489 | GM1 gangliosidosis type 3 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
|
||
| DOID:8893 | psoriasis | HGNC:320 | Homo sapiens (human) | 177 | AGER |
|
||
| DOID:3312 | bipolar disorder | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
|
||
| DOID:1909 | melanoma | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
|
||
| DOID:4448 | macular degeneration | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
|
||
| DOID:9975 | cocaine dependence | HGNC:1963 | Homo sapiens (human) | 1142 | CHRNB3 |
|
||
| DOID:635 | acquired immunodeficiency syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
|
||
| DOID:0050861 | colorectal adenocarcinoma | HGNC:25032 | Homo sapiens (human) | 338094 | FAM151A |
|
||
| DOID:0080430 | developmental and epileptic encephalopathy 65 | HGNC:13760 | Homo sapiens (human) | 26999 | CYFIP2 |
|
||
| DOID:0070233 | Loeys-Dietz syndrome 4 | HGNC:11768 | Homo sapiens (human) | 7042 | TGFB2 |
|
||
| DOID:13550 | angle-closure glaucoma | HGNC:6665 | Homo sapiens (human) | 4016 | LOXL1 |
|
||
| DOID:0050580 | hereditary lymphedema | HGNC:28993 | Homo sapiens (human) | 9780 | PIEZO1 |
|
||
| DOID:0090081 | hypogonadotropic hypogonadism 22 with or without anosmia | HGNC:22788 | Homo sapiens (human) | 389549 | FEZF1 |
|
||
| DOID:12859 | choreatic disease | HGNC:11825 | Homo sapiens (human) | 7080 | NKX2-1 |
|
||
| DOID:3227 | tracheal stenosis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
|
||
| DOID:10003 | sensorineural hearing loss | HGNC:7605 | Homo sapiens (human) | 4646 | MYO6 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
|
||
| DOID:0110771 | hereditary spastic paraplegia 18 | HGNC:1356 | Homo sapiens (human) | 11160 | ERLIN2 |
|
||
| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
|
||
| DOID:0110402 | retinitis pigmentosa 45 | HGNC:2151 | Homo sapiens (human) | 1258 | CNGB1 |
|
||
| DOID:5082 | liver cirrhosis | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
|
||
| DOID:612 | primary immunodeficiency disease | HGNC:16391 | Homo sapiens (human) | 64170 | CARD9 |
|
