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
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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9538 | multiple myeloma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:8552 | chronic myeloid leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:12858 | Huntington's disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:0112298 | spondylometaphyseal dysplasia Sedaghatian type | SGD:S000001509 | Saccharomyces cerevisiae S288C | 853842 | GPX1 |
|
||
| DOID:9119 | acute myeloid leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:11714 | gestational diabetes | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:0050083 | Keshan disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
|
||
| DOID:3454 | brain infarction | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
|
||
| DOID:0060680 | pigment dispersion syndrome | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
|
||
| DOID:0111630 | familial erythrocytosis 8 | SGD:S000001635 | Saccharomyces cerevisiae S288C | 853705 | GPM1 |
|
||
| DOID:0080108 | myoglobinuria | SGD:S000001635 | Saccharomyces cerevisiae S288C | 853705 | GPM1 |
|
||
| DOID:0111420 | familial GPIHBP1 deficiency | HGNC:24945 | Homo sapiens (human) | 338328 | GPIHBP1 |
|
||
| DOID:0081223 | glycosylphosphatidylinositol biosynthesis defect 16 | SGD:S000005997 | Saccharomyces cerevisiae S288C | 856029 | GPI2 |
|
||
| DOID:0080283 | developmental and epileptic encephalopathy 55 | SGD:S000002845 | Saccharomyces cerevisiae S288C | 852047 | GPI19 |
|
||
| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | SGD:S000000208 | Saccharomyces cerevisiae S288C | 852289 | GPI18 |
|
||
| DOID:10112 | sleeping sickness | SGD:S000003110 | Saccharomyces cerevisiae S288C | 852735 | GPI10 |
|
||
| DOID:0112216 | developmental and epileptic encephalopathy 80 | SGD:S000003110 | Saccharomyces cerevisiae S288C | 852735 | GPI10 |
|
||
| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | SGD:S000003448 | Saccharomyces cerevisiae S288C | 853130 | GPI1 |
|
||
| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
|
||
| DOID:14330 | Parkinson's disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
|
||
| DOID:9119 | acute myeloid leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
|
||
| DOID:9952 | acute lymphoblastic leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
|
||
| DOID:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
|
