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:0081397 | Vissers-Bodmer syndrome | HGNC:7877 | Homo sapiens (human) | 23019 | CNOT1 |
|
||
| DOID:0081398 | holoprosencephaly 12 | HGNC:7877 | Homo sapiens (human) | 23019 | CNOT1 |
|
||
| DOID:114 | heart disease | HGNC:7877 | Homo sapiens (human) | 23019 | CNOT1 |
|
||
| DOID:0111404 | Jalili syndrome | HGNC:105 | Homo sapiens (human) | 26504 | CNNM4 |
|
||
| DOID:0060884 | renal hypomagnesemia 6 | HGNC:103 | Homo sapiens (human) | 54805 | CNNM2 |
|
||
| DOID:5419 | schizophrenia | HGNC:103 | Homo sapiens (human) | 54805 | CNNM2 |
|
||
| DOID:0080242 | syndromic X-linked mental retardation Hough type | HGNC:19701 | Homo sapiens (human) | 22866 | CNKSR2 |
|
||
| DOID:10584 | retinitis pigmentosa | HGNC:2151 | Homo sapiens (human) | 1258 | CNGB1 |
|
||
| DOID:0110402 | retinitis pigmentosa 45 | HGNC:2151 | Homo sapiens (human) | 1258 | CNGB1 |
|
||
| DOID:13399 | color blindness | HGNC:2150 | Homo sapiens (human) | 1261 | CNGA3 |
|
||
| DOID:0110007 | achromatopsia 2 | HGNC:2150 | Homo sapiens (human) | 1261 | CNGA3 |
|
||
| DOID:0110377 | retinitis pigmentosa 49 | HGNC:2148 | Homo sapiens (human) | 1259 | CNGA1 |
|
||
| DOID:10584 | retinitis pigmentosa | HGNC:2148 | Homo sapiens (human) | 1259 | CNGA1 |
|
||
| DOID:9970 | obesity | SGD:S000000054 | Saccharomyces cerevisiae S288C | 851241 | CNE1 |
|
||
| DOID:2921 | glomerulonephritis | HGNC:20675 | Homo sapiens (human) | 84735 | CNDP1 |
|
||
| DOID:0060307 | autosomal dominant intellectual developmental disorder | SGD:S000005619 | Saccharomyces cerevisiae S288C | 854260 | CMR2 |
|
||
| DOID:3908 | lung non-small cell carcinoma | HGNC:18170 | Homo sapiens (human) | 51727 | CMPK1 |
|
||
| DOID:162 | cancer | HGNC:18170 | Homo sapiens (human) | 51727 | CMPK1 |
|
||
| DOID:1312 | focal segmental glomerulosclerosis | HGNC:18290 | Homo sapiens (human) | 55907 | CMAS |
|
||
| DOID:3310 | atopic dermatitis | HGNC:2097 | Homo sapiens (human) | 1215 | CMA1 |
|
||
| DOID:1591 | renovascular hypertension | HGNC:2097 | Homo sapiens (human) | 1215 | CMA1 |
|
||
| DOID:11335 | sarcoidosis | HGNC:2097 | Homo sapiens (human) | 1215 | CMA1 |
|
||
| DOID:3082 | interstitial lung disease | HGNC:2097 | Homo sapiens (human) | 1215 | CMA1 |
|
||
| DOID:2841 | asthma | HGNC:2097 | Homo sapiens (human) | 1215 | CMA1 |
|
||
| DOID:1682 | congenital heart disease | HGNC:2097 | Homo sapiens (human) | 1215 | CMA1 |
|
