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:0050650 | familial atrial fibrillation | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
|
||
| DOID:0080784 | urinary tract infection | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
|
||
| DOID:2581 | chondrodysplasia punctata | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
|
||
| DOID:13189 | gout | HGNC:10931 | Homo sapiens (human) | 10786 | SLC17A3 |
|
||
| DOID:6543 | acne | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
|
||
| DOID:0110066 | amelogenesis imperfecta type 1G | HGNC:23015 | Homo sapiens (human) | 54757 | FAM20A |
|
||
| DOID:3393 | coronary artery disease | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
|
||
| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
|
||
| DOID:0060074 | ductal carcinoma in situ | HGNC:9955 | Homo sapiens (human) | 5970 | RELA |
|
||
| DOID:0060584 | Noonan syndrome 6 | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
|
||
| DOID:0080470 | developmental and epileptic encephalopathy 36 | HGNC:30881 | Homo sapiens (human) | 79868 | ALG13 |
|
||
| DOID:0110384 | retinitis pigmentosa 25 | HGNC:21555 | Homo sapiens (human) | 346007 | EYS |
|
||
| DOID:0112181 | Schinzel type phocomelia | HGNC:12786 | Homo sapiens (human) | 7476 | WNT7A |
|
||
| DOID:1612 | breast cancer | HGNC:16696 | Homo sapiens (human) | 22938 | SNW1 |
|
||
| DOID:0050548 | hereditary sensory neuropathy | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
|
||
| DOID:0060449 | gelatinous drop-like corneal dystrophy | HGNC:11530 | Homo sapiens (human) | 4070 | TACSTD2 |
|
||
| DOID:1037 | lymphoid leukemia | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
|
||
| DOID:0110178 | Charcot-Marie-Tooth disease axonal type 2V | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
|
||
| DOID:1287 | cardiovascular system disease | HGNC:16808 | Homo sapiens (human) | 197131 | UBR1 |
|
||
| DOID:0111562 | overhydrated hereditary stomatocytosis | HGNC:10006 | Homo sapiens (human) | 6005 | RHAG |
|
||
| DOID:13141 | uveitis | HGNC:5234 | Homo sapiens (human) | 3305 | HSPA1L |
|
||
| DOID:0112262 | leucine-sensitive hypoglycemia of infancy | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
|
||
| DOID:2559 | opiate dependence | HGNC:8153 | Homo sapiens (human) | 4985 | OPRD1 |
|
||
| DOID:9970 | obesity | HGNC:7670 | Homo sapiens (human) | 8202 | NCOA3 |
|
||
| DOID:3407 | carotid artery disease | HGNC:1869 | Homo sapiens (human) | 1071 | CETP |
|
