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:1094 | attention deficit hyperactivity disorder | HGNC:2989 | Homo sapiens (human) | 1795 | DOCK3 |
|
||
| DOID:2531 | hematologic cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
|
||
| DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
|
||
| DOID:13963 | nuclear senile cataract | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
|
||
| DOID:0080600 | COVID-19 | HGNC:7 | Homo sapiens (human) | 2 | A2M |
|
||
| DOID:0110819 | hereditary spastic paraplegia 74 | HGNC:27302 | Homo sapiens (human) | 200205 | IBA57 |
|
||
| DOID:13359 | Ehlers-Danlos syndrome | HGNC:218 | Homo sapiens (human) | 9509 | ADAMTS2 |
|
||
| DOID:0060879 | primary hypomagnesemia | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
|
||
| DOID:3310 | atopic dermatitis | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
|
||
| DOID:3393 | coronary artery disease | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
|
||
| DOID:0080526 | bronchiectasis 1 | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
|
||
| DOID:0080280 | gingival fibromatosis 5 | HGNC:9966 | Homo sapiens (human) | 5978 | REST |
|
||
| DOID:9261 | nasopharynx carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
|
||
| DOID:8692 | myeloid leukemia | HGNC:12767 | Homo sapiens (human) | 54904 | NSD3 |
|
||
| DOID:4441 | dysgerminoma | HGNC:6342 | Homo sapiens (human) | 3815 | KIT |
|
||
| DOID:655 | inherited metabolic disorder | HGNC:14409 | Homo sapiens (human) | 60386 | SLC25A19 |
|
||
| DOID:12971 | hereditary spherocytosis | HGNC:3381 | Homo sapiens (human) | 2038 | EPB42 |
|
||
| DOID:0050784 | primary progressive multiple sclerosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
|
||
| DOID:2957 | pulmonary tuberculosis | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
|
||
| DOID:437 | myasthenia gravis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
|
||
| DOID:12849 | autistic disorder | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
|
||
| DOID:3008 | invasive ductal carcinoma | HGNC:10473 | Homo sapiens (human) | 864 | RUNX3 |
|
||
| DOID:5408 | Paget's disease of bone | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
|
||
| DOID:399 | tuberculosis | HGNC:3443 | Homo sapiens (human) | 2069 | EREG |
|
||
| DOID:0050963 | spinocerebellar ataxia type 13 | HGNC:6235 | Homo sapiens (human) | 3748 | KCNC3 |
|
