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:0060856 | right atrial isomerism | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
|
||
| DOID:14323 | Marfan syndrome | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
|
||
| DOID:0050787 | juvenile polyposis syndrome | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
|
||
| DOID:10591 | pre-eclampsia | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
|
||
| DOID:0050545 | visceral heterotaxy | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
|
||
| DOID:0081146 | common variable immunodeficiency 3 | HGNC:1633 | Homo sapiens (human) | 930 | CD19 |
|
||
| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:20313 | Homo sapiens (human) | 93035 | PKHD1L1 |
|
||
| DOID:0081148 | common variable immunodeficiency 5 | HGNC:7315 | Homo sapiens (human) | 931 | MS4A1 |
|
||
| DOID:2921 | glomerulonephritis | HGNC:7315 | Homo sapiens (human) | 931 | MS4A1 |
|
||
| DOID:0050741 | alcohol dependence | HGNC:6232 | Homo sapiens (human) | 9312 | KCNB2 |
|
||
| DOID:11984 | hypertrophic cardiomyopathy | HGNC:28185 | Homo sapiens (human) | 93129 | ORAI3 |
|
||
| DOID:12930 | dilated cardiomyopathy | HGNC:28185 | Homo sapiens (human) | 93129 | ORAI3 |
|
||
| DOID:0110060 | amelogenesis imperfecta hypomaturation type 2A2 | HGNC:7167 | Homo sapiens (human) | 9313 | MMP20 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:6348 | Homo sapiens (human) | 9314 | KLF4 |
|
||
| DOID:0080689 | mosaic variegated aneuploidy syndrome 3 | HGNC:12307 | Homo sapiens (human) | 9319 | TRIP13 |
|
||
| DOID:162 | cancer | HGNC:12306 | Homo sapiens (human) | 9320 | TRIP12 |
|
||
| DOID:0080234 | Clark-Baraitser syndrome | HGNC:12306 | Homo sapiens (human) | 9320 | TRIP12 |
|
||
| DOID:0080054 | achondrogenesis type IA | HGNC:12305 | Homo sapiens (human) | 9321 | TRIP11 |
|
||
| DOID:0070436 | hyperphosphatasia with impaired intellectual development syndrome 4 | HGNC:23719 | Homo sapiens (human) | 93210 | PGAP3 |
|
||
| DOID:12858 | Huntington's disease | HGNC:12304 | Homo sapiens (human) | 9322 | TRIP10 |
|
||
| DOID:0050745 | diffuse large B-cell lymphoma | HGNC:1643 | Homo sapiens (human) | 933 | CD22 |
|
||
| DOID:2377 | multiple sclerosis | HGNC:929 | Homo sapiens (human) | 9331 | B4GALT6 |
|
||
| DOID:9146 | visceral leishmaniasis | HGNC:1631 | Homo sapiens (human) | 9332 | CD163 |
|
||
| DOID:0081292 | traumatic brain injury | HGNC:1631 | Homo sapiens (human) | 9332 | CD163 |
|
||
| DOID:10887 | lepromatous leprosy | HGNC:1631 | Homo sapiens (human) | 9332 | CD163 |
|
