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
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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:5419 | schizophrenia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
|
||
| DOID:2256 | osteochondrodysplasia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
|
||
| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
|
||
| DOID:0112152 | CHIME syndrome | HGNC:8966 | Homo sapiens (human) | 9487 | PIGL |
|
||
| DOID:0112216 | developmental and epileptic encephalopathy 80 | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
|
||
| DOID:10112 | sleeping sickness | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
|
||
| DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
|
||
| DOID:8893 | psoriasis | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
|
||
| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
|
||
| DOID:9744 | type 1 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
|
||
| DOID:0050889 | non-syndromic intellectual disability | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
|
||
| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
|
||
| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
|
||
| DOID:326 | ischemia | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:11624 | penile benign neoplasm | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:2671 | transitional cell carcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:2615 | papilloma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:9206 | Barrett's esophagus | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:13976 | peptic esophagitis | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:2870 | endometrial adenocarcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:2152 | ovary epithelial cancer | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:3908 | lung non-small cell carcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:0060074 | ductal carcinoma in situ | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
||
| DOID:289 | endometriosis | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
|
