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:11446 | sciatic neuropathy | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
|
||
| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
|
||
| DOID:2154 | nephroblastoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
|
||
| DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
|
||
| DOID:0111756 | Leber hereditary optic neuropathy with demyelinating disease of CNS | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
|
||
| DOID:5723 | optic atrophy | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
|
||
| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
|
||
| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
|
||
| DOID:9452 | steatotic liver disease | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
|
||
| DOID:9970 | obesity | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
|
||
| DOID:906 | peroxisomal disease | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
|
||
| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
|
||
| DOID:14701 | propionic acidemia | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
|
||
| DOID:9252 | amino acid metabolic disorder | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
|
||
| DOID:9252 | amino acid metabolic disorder | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
|
||
| DOID:14701 | propionic acidemia | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
|
||
| DOID:3651 | pyruvate carboxylase deficiency disease | HGNC:8636 | Homo sapiens (human) | 5091 | PC |
|
||
| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
|
||
| DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
|
||
| DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
|
||
| DOID:12305 | Bloch-Sulzberger syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
|
||
| DOID:162 | cancer | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
|
||
| DOID:4137 | common bile duct disease | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
|
