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:0070154 | hereditary sensory neuropathy type 1F | HGNC:24526 | Homo sapiens (human) | 25923 | ATL3 |
|
||
| DOID:2219 | Glanzmann's thrombasthenia | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
|
||
| DOID:0050742 | nicotine dependence | HGNC:1958 | Homo sapiens (human) | 1137 | CHRNA4 |
|
||
| DOID:0060037 | developmental disorder of mental health | HGNC:11526 | Homo sapiens (human) | 6869 | TACR1 |
|
||
| DOID:1070 | primary open angle glaucoma | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
|
||
| DOID:3312 | bipolar disorder | HGNC:1963 | Homo sapiens (human) | 1142 | CHRNB3 |
|
||
| DOID:8923 | skin melanoma | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
|
||
| DOID:10534 | stomach cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
|
||
| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:2342 | Homo sapiens (human) | 1384 | CRAT |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
|
||
| DOID:14330 | Parkinson's disease | HGNC:6367 | Homo sapiens (human) | 5653 | KLK6 |
|
||
| DOID:2957 | pulmonary tuberculosis | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
|
||
| DOID:0070197 | distal myopathy 1 | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
|
||
| DOID:1825 | childhood absence epilepsy | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
|
||
| DOID:811 | lipodystrophy | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
|
||
| DOID:1496 | echinococcosis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
|
||
| DOID:12662 | paracoccidioidomycosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0080237 | autosomal dominant intellectual developmental disorder 46 | HGNC:6299 | Homo sapiens (human) | 56479 | KCNQ5 |
|
||
| DOID:0110591 | autosomal dominant nonsyndromic deafness 7 | HGNC:6653 | Homo sapiens (human) | 4009 | LMX1A |
|
||
| DOID:9952 | acute lymphoblastic leukemia | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
|
||
| DOID:0110157 | Charcot-Marie-Tooth disease type 2J | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
|
||
| DOID:9206 | Barrett's esophagus | HGNC:7376 | Homo sapiens (human) | 4481 | MSR1 |
|
||
| DOID:0111512 | metachondromatosis | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
|
||
| DOID:10603 | glucose intolerance | HGNC:610 | Homo sapiens (human) | 345 | APOC3 |
|
||
| DOID:10763 | hypertension | HGNC:11769 | Homo sapiens (human) | 7043 | TGFB3 |
|
