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:0080507 | Cornelia de Lange syndrome 3 | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
|
||
| DOID:0090019 | sitosterolemia | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
|
||
| DOID:2236 | congenital afibrinogenemia | HGNC:3661 | Homo sapiens (human) | 2243 | FGA |
|
||
| DOID:0110033 | autosomal recessive Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:0080050 | acromesomelic dysplasia, Maroteaux type | HGNC:7944 | Homo sapiens (human) | 4882 | NPR2 |
|
||
| DOID:0111064 | autosomal recessive distal hereditary motor neuronopathy 1 | HGNC:5542 | Homo sapiens (human) | 3508 | IGHMBP2 |
|
||
| DOID:10763 | hypertension | HGNC:7940 | Homo sapiens (human) | 4879 | NPPB |
|
||
| DOID:0050848 | obstructive sleep apnea | HGNC:3179 | Homo sapiens (human) | 1909 | EDNRA |
|
||
| DOID:0110596 | primary ciliary dyskinesia 21 | HGNC:24245 | Homo sapiens (human) | 92749 | DRC1 |
|
||
| DOID:0080570 | congenital disorder of glycosylation It | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
|
||
| DOID:1094 | attention deficit hyperactivity disorder | HGNC:11049 | Homo sapiens (human) | 6531 | SLC6A3 |
|
||
| DOID:0070068 | autosomal dominant intellectual developmental disorder 38 | HGNC:3192 | Homo sapiens (human) | 1917 | EEF1A2 |
|
||
| DOID:13515 | tuberous sclerosis | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
|
||
| DOID:10763 | hypertension | HGNC:1030 | Homo sapiens (human) | 624 | BDKRB2 |
|
||
| DOID:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
|
||
| DOID:12894 | Sjogren's syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0080021 | Schmid metaphyseal chondrodysplasia | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
|
||
| DOID:0081364 | neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
|
||
| DOID:12120 | pulmonary alveolar proteinosis | HGNC:2436 | Homo sapiens (human) | 1439 | CSF2RB |
|
||
| DOID:0111194 | autosomal dominant adult-onset proximal spinal muscular atrophy | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
|
||
| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:933 | Homo sapiens (human) | 23621 | BACE1 |
|
||
| DOID:10763 | hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0060486 | Perry syndrome | HGNC:2711 | Homo sapiens (human) | 1639 | DCTN1 |
|
||
| DOID:0060741 | methylmalonic acidemia due to transcobalamin receptor defect | HGNC:16692 | Homo sapiens (human) | 51293 | CD320 |
|
