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:0111945 | immunodeficiency 31A | HGNC:11362 | Homo sapiens (human) | 6772 | STAT1 |
|
||
| DOID:0111902 | thrombophilia due to activated protein C resistance | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
|
||
| DOID:0080234 | Clark-Baraitser syndrome | HGNC:12306 | Homo sapiens (human) | 9320 | TRIP12 |
|
||
| DOID:0060781 | congenital secretory sodium diarrhea 3 | HGNC:11247 | Homo sapiens (human) | 10653 | SPINT2 |
|
||
| DOID:0111025 | cone-rod dystrophy 19 | HGNC:19963 | Homo sapiens (human) | 23093 | TTLL5 |
|
||
| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
|
||
| DOID:0060558 | lethal congenital contracture syndrome | HGNC:8011 | Homo sapiens (human) | 8506 | CNTNAP1 |
|
||
| DOID:0070187 | Y-linked spermatogenic failure 2 | HGNC:12633 | Homo sapiens (human) | 8287 | USP9Y |
|
||
| DOID:4450 | renal cell carcinoma | HGNC:30064 | Homo sapiens (human) | 55193 | PBRM1 |
|
||
| DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | HGNC:28596 | Homo sapiens (human) | 148789 | B3GALNT2 |
|
||
| DOID:0110946 | autosomal recessive osteopetrosis 7 | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
|
||
| DOID:0081220 | autosomal recessive intellectual developmental disorder 58 | HGNC:18248 | Homo sapiens (human) | 55250 | ELP2 |
|
||
| DOID:0112091 | nuclear type mitochondrial complex I deficiency 34 | HGNC:33551 | Homo sapiens (human) | 284184 | NDUFAF8 |
|
||
| DOID:891 | progressive myoclonus epilepsy | HGNC:10739 | Homo sapiens (human) | 10501 | SEMA6B |
|
||
| DOID:0111999 | immunodeficiency 61 | HGNC:13867 | Homo sapiens (human) | 30011 | SH3KBP1 |
|
||
| DOID:0111576 | dehydrated hereditary stomatocytosis 1 | HGNC:28993 | Homo sapiens (human) | 9780 | PIEZO1 |
|
||
| DOID:0080679 | neuronal intestinal dysplasia type A | HGNC:3431 | Homo sapiens (human) | 2065 | ERBB3 |
|
||
| DOID:0111665 | ectodermal dysplasia 10B | HGNC:2895 | Homo sapiens (human) | 10913 | EDAR |
|
||
| DOID:0090088 | hypogonadotropic hypogonadism 24 without anosmia | HGNC:3964 | Homo sapiens (human) | 2488 | FSHB |
|
||
| DOID:13809 | familial combined hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
|
||
| DOID:5419 | schizophrenia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
|
||
| DOID:0070409 | autosomal recessive spinocerebellar ataxia 28 | HGNC:26053 | Homo sapiens (human) | 54974 | THG1L |
|
||
| DOID:936 | brain disease | HGNC:13481 | Homo sapiens (human) | 81622 | UNC93B1 |
|
||
| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:26178 | Homo sapiens (human) | 80206 | FHOD3 |
|
