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:3748 | esophagus squamous cell carcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
|
||
| DOID:8955 | sideroblastic anemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
|
||
| DOID:3910 | lung adenocarcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
|
||
| DOID:2224 | essential thrombocythemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
|
||
| DOID:0050731 | vitamin B12 deficiency | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
|
||
| DOID:13564 | aspergillosis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
|
||
| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
|
||
| DOID:14250 | Down syndrome | HGNC:14683 | Homo sapiens (human) | 23275 | POFUT2 |
|
||
| DOID:9970 | obesity | HGNC:1473 | Homo sapiens (human) | 821 | CANX |
|
||
| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
|
||
| DOID:9256 | colorectal cancer | HGNC:14897 | Homo sapiens (human) | 80271 | ITPKC |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14932 | Homo sapiens (human) | 23409 | SIRT4 |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:224 | transient cerebral ischemia | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:3911 | progeria | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:9970 | obesity | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
|
||
| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
|
||
| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
|
||
| DOID:1574 | alcohol use disorder | HGNC:14942 | Homo sapiens (human) | 79660 | PPP1R3B |
|
||
| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
|
||
| DOID:1459 | hypothyroidism | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
|
||
| DOID:10825 | essential hypertension | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
|
||
| DOID:161 | keratosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
|
||
| DOID:0060180 | colitis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
|
