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:4001 | ovarian carcinoma | HGNC:3176 | Homo sapiens (human) | 1906 | EDN1 |
|
||
| DOID:14789 | spondyloepiphyseal dysplasia congenita | MGI:1337006 | Mus musculus (house mouse) | 12950 | Hapln1 |
|
||
| DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | MGI:104696 | Mus musculus (house mouse) | 20277 | Scnn1b |
|
||
| DOID:2475 | chronic conjunctivitis | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
|
||
| DOID:5419 | schizophrenia | HGNC:8039 | Homo sapiens (human) | 4923 | NTSR1 |
|
||
| DOID:12236 | primary biliary cholangitis | RGD:620925 | Rattus norvegicus (Norway rat) | 83516 | Ppargc1a |
|
||
| DOID:0060892 | late onset Parkinson's disease | HGNC:7106 | Homo sapiens (human) | 4287 | ATXN3 |
|
||
| DOID:0111050 | Quebec platelet disorder | HGNC:9052 | Homo sapiens (human) | 5328 | PLAU |
|
||
| DOID:0081345 | congenital myopathy 10B | HGNC:29634 | Homo sapiens (human) | 84466 | MEGF10 |
|
||
| DOID:0070024 | autosomal recessive dyskeratosis congenita 6 | HGNC:8609 | Homo sapiens (human) | 5073 | PARN |
|
||
| DOID:0060704 | lymphoproliferative syndrome | HGNC:11937 | Homo sapiens (human) | 970 | CD70 |
|
||
| DOID:0070012 | Seckel syndrome 5 | HGNC:29298 | Homo sapiens (human) | 22995 | CEP152 |
|
||
| DOID:0111162 | epidermal nevus | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
|
||
| DOID:0110959 | Gaucher's disease type III | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
|
||
| DOID:0070340 | classic citrullinemia | HGNC:758 | Homo sapiens (human) | 445 | ASS1 |
|
||
| DOID:0110708 | hypotrichosis 11 | HGNC:11161 | Homo sapiens (human) | 6635 | SNRPE |
|
||
| DOID:0111094 | Fanconi anemia complementation group N | HGNC:26144 | Homo sapiens (human) | 79728 | PALB2 |
|
||
| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:20313 | Homo sapiens (human) | 93035 | PKHD1L1 |
|
||
| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
|
||
| DOID:9119 | acute myeloid leukemia | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
|
||
| DOID:0111887 | Diamond-blackfan anemia 3 | HGNC:10411 | Homo sapiens (human) | 6229 | RPS24 |
|
||
| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
|
||
| DOID:0080746 | Sweet syndrome | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
|
||
| DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
|
||
| DOID:10123 | pigmentation disease | HGNC:12450 | Homo sapiens (human) | 7306 | TYRP1 |
|
