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:0060870 | isolated growth hormone deficiency | RGD:621397 | Rattus norvegicus (Norway rat) | 84022 | Ghsr |
|
||
| DOID:0060869 | late-onset retinal degeneration | MGI:2385958 | Mus musculus (house mouse) | 235312 | C1qtnf5 |
|
||
| DOID:0060868 | leukoencephalopathy with vanishing white matter | MGI:95300 | Mus musculus (house mouse) | 13667 | Eif2b4 |
|
||
| DOID:0060868 | leukoencephalopathy with vanishing white matter | SGD:S000003315 | Saccharomyces cerevisiae S288C | 852974 | GCD2 |
|
||
| DOID:0060868 | leukoencephalopathy with vanishing white matter | HGNC:3257 | Homo sapiens (human) | 1967 | EIF2B1 |
|
||
| DOID:0060868 | leukoencephalopathy with vanishing white matter | MGI:2446176 | Mus musculus (house mouse) | 224045 | Eif2b5 |
|
||
| DOID:0060868 | leukoencephalopathy with vanishing white matter | HGNC:3260 | Homo sapiens (human) | 8890 | EIF2B4 |
|
||
| DOID:0060867 | macrocephaly-autism syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
|
||
| DOID:0060866 | patterned macular dystrophy 1 | Xenbase:XB-GENE-17339014 | Xenopus laevis (African clawed frog) | 398002 | prph2.S |
|
||
| DOID:0060866 | patterned macular dystrophy 1 | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
|
||
| DOID:0060866 | patterned macular dystrophy 1 | RGD:3549 | Rattus norvegicus (Norway rat) | 25534 | Prph2 |
|
||
| DOID:0060866 | patterned macular dystrophy 1 | MGI:102791 | Mus musculus (house mouse) | 19133 | Prph2 |
|
||
| DOID:0060864 | patterned macular dystrophy 2 | HGNC:2509 | Homo sapiens (human) | 1495 | CTNNA1 |
|
||
| DOID:0060863 | patterned macular dystrophy | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
|
||
| DOID:0060863 | patterned macular dystrophy | RGD:3549 | Rattus norvegicus (Norway rat) | 25534 | Prph2 |
|
||
| DOID:0060863 | patterned macular dystrophy | Xenbase:XB-GENE-17339014 | Xenopus laevis (African clawed frog) | 398002 | prph2.S |
|
||
| DOID:0060863 | patterned macular dystrophy | MGI:102791 | Mus musculus (house mouse) | 19133 | Prph2 |
|
||
| DOID:0060861 | microphthalmia with limb anomalies | MGI:1929878 | Mus musculus (house mouse) | 64075 | Smoc1 |
|
||
| DOID:0060861 | microphthalmia with limb anomalies | HGNC:20318 | Homo sapiens (human) | 64093 | SMOC1 |
|
||
| DOID:0060859 | salmonellosis | HGNC:5970 | Homo sapiens (human) | 3593 | IL12B |
|
||
| DOID:0060859 | salmonellosis | MGI:96540 | Mus musculus (house mouse) | 16160 | Il12b |
|
||
| DOID:0060858 | hypotonia-cystinuria syndrome | HGNC:26276 | Homo sapiens (human) | 79823 | CAMKMT |
|
||
| DOID:0060856 | right atrial isomerism | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
|
||
| DOID:0060856 | right atrial isomerism | MGI:87912 | Mus musculus (house mouse) | 11481 | Acvr2b |
|
||
| DOID:0060856 | right atrial isomerism | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
|
