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:0070430 | combined oxidative phosphorylation deficiency 57 | HGNC:16148 | Homo sapiens (human) | 54675 | CRLS1 |
|
||
| DOID:234 | colon adenocarcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
|
||
| DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
|
||
| DOID:178 | vascular disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
|
||
| DOID:0050861 | colorectal adenocarcinoma | HGNC:12020 | Homo sapiens (human) | 8460 | TPST1 |
|
||
| DOID:2154 | nephroblastoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
|
||
| DOID:0110242 | cataract 13 with adult i phenotype | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
|
||
| DOID:0080414 | developmental and epileptic encephalopathy 15 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
|
||
| DOID:0111393 | mucopolysaccharidosis type IIIC | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
|
||
| DOID:9976 | heroin dependence | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
|
||
| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
|
||
| DOID:0080665 | warfarin resistance | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
|
||
| DOID:9119 | acute myeloid leukemia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
|
||
| DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
|
||
| DOID:1612 | breast cancer | HGNC:2873 | Homo sapiens (human) | 1727 | CYB5R3 |
|
||
| DOID:12361 | Graves' disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
|
||
| DOID:2237 | hepatitis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
|
||
| DOID:0110196 | Charcot-Marie-Tooth disease type 4G | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
|
||
| DOID:4247 | coronary restenosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0050700 | cardiomyopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
|
||
| DOID:7147 | ankylosing spondylitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
|
||
| DOID:12306 | vitiligo | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
|
||
| DOID:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
|
||
| DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
|
||
| DOID:2871 | endometrial carcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
|
