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:854 | collagen disease | HGNC:2207 | Homo sapiens (human) | 1287 | COL4A5 |
|
||
| DOID:10983 | Alport syndrome | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
|
||
| DOID:783 | end stage renal disease | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
|
||
| DOID:854 | collagen disease | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
|
||
| DOID:0110033 | autosomal recessive Alport syndrome | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
|
||
| DOID:0111365 | benign familial hematuria | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
|
||
| DOID:423 | myopathy | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
|
||
| DOID:0110033 | autosomal recessive Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:2921 | glomerulonephritis | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:783 | end stage renal disease | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:854 | collagen disease | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:423 | myopathy | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:10983 | Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:0110032 | autosomal dominant Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:0111365 | benign familial hematuria | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
|
||
| DOID:0060263 | porencephaly | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
|
||
| DOID:13223 | uterine fibroid | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
|
||
| DOID:0112314 | brain small vessel disease 2 | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
|
||
| DOID:13129 | severe pre-eclampsia | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
|
||
| DOID:1936 | atherosclerosis | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
|
||
| DOID:5844 | myocardial infarction | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
|
||
| DOID:9970 | obesity | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
|
||
| DOID:0060263 | porencephaly | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
|
||
| DOID:557 | kidney disease | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
|
||
| DOID:13223 | uterine fibroid | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
|
