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 / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
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:9352 | type 2 diabetes mellitus | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
|
||
| DOID:9074 | systemic lupus erythematosus | HGNC:2956 | Homo sapiens (human) | 1773 | DNASE1 |
|
||
| DOID:0060900 | Parkinson's disease 14 | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
|
||
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
|
||
| DOID:0110497 | autosomal recessive nonsyndromic deafness 39 | HGNC:4893 | Homo sapiens (human) | 3082 | HGF |
|
||
| DOID:10763 | hypertension | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
|
||
| DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
|
||
| DOID:2962 | Cockayne syndrome | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
|
||
| DOID:0060688 | arteriovenous malformations of the brain | HGNC:3349 | Homo sapiens (human) | 2022 | ENG |
|
||
| DOID:2908 | Treacher Collins syndrome | HGNC:11654 | Homo sapiens (human) | 6949 | TCOF1 |
|
||
| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
|
||
| DOID:0110156 | Charcot-Marie-Tooth disease type 2B1 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
|
||
| DOID:0111066 | congenital bile acid synthesis defect 5 | HGNC:67 | Homo sapiens (human) | 5825 | ABCD3 |
|
||
| DOID:0110334 | osteogenesis imperfecta type 1 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
|
||
| DOID:0060810 | syndromic X-linked intellectual disability type 10 | HGNC:4800 | Homo sapiens (human) | 3028 | HSD17B10 |
|
||
| DOID:0050629 | Aicardi-Goutieres syndrome | HGNC:15925 | Homo sapiens (human) | 25939 | SAMHD1 |
|
||
| DOID:0060903 | thrombosis | HGNC:775 | Homo sapiens (human) | 462 | SERPINC1 |
|
||
| DOID:3650 | lactic acidosis | RGD:620687 | Rattus norvegicus (Norway rat) | 64035 | Pygl |
|
||
| DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
|
||
| DOID:0060733 | junctional epidermolysis bullosa with pyloric atresia | HGNC:6158 | Homo sapiens (human) | 3691 | ITGB4 |
|
||
| DOID:594 | panic disorder | HGNC:5286 | Homo sapiens (human) | 3350 | HTR1A |
|
||
| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
|
||
| DOID:1287 | cardiovascular system disease | HGNC:320 | Homo sapiens (human) | 177 | AGER |
|
||
| DOID:14451 | hyperkalemic periodic paralysis | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
|
||
| DOID:0111194 | autosomal dominant adult-onset proximal spinal muscular atrophy | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
|
