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:0110587 | autosomal dominant nonsyndromic deafness 66 | HGNC:1632 | Homo sapiens (human) | 8763 | CD164 |
|
||
| DOID:2280 | hidradenitis suppurativa | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0080379 | nephrotic syndrome type 2 | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
|
||
| DOID:1287 | cardiovascular system disease | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
|
||
| DOID:2048 | autoimmune hepatitis | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
|
||
| DOID:0080633 | developmental cardiac valvular defect | HGNC:7432 | Homo sapiens (human) | 4522 | MTHFD1 |
|
||
| DOID:0080981 | arthrogryposis multiplex congenita-5 | HGNC:3098 | Homo sapiens (human) | 1861 | TOR1A |
|
||
| DOID:1749 | squamous cell carcinoma | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
|
||
| DOID:0060227 | Adams-Oliver syndrome | HGNC:28526 | Homo sapiens (human) | 285203 | EOGT |
|
||
| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:5035 | Homo sapiens (human) | 3183 | HNRNPC |
|
||
| DOID:0111959 | immunodeficiency 15B | HGNC:5960 | Homo sapiens (human) | 3551 | IKBKB |
|
||
| DOID:0081235 | autosomal recessive intellectual developmental disorder 76 | HGNC:4571 | Homo sapiens (human) | 2890 | GRIA1 |
|
||
| DOID:10003 | sensorineural hearing loss | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
|
||
| DOID:591 | phobic disorder | HGNC:11957 | Homo sapiens (human) | 9968 | MED12 |
|
||
| DOID:0080600 | COVID-19 | HGNC:9075 | Homo sapiens (human) | 5345 | SERPINF2 |
|
||
| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
|
||
| DOID:0111768 | X-linked properdin deficiency | HGNC:8864 | Homo sapiens (human) | 5199 | CFP |
|
||
| DOID:1612 | breast cancer | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
|
||
| DOID:0080844 | omodysplasia 1 | HGNC:4454 | Homo sapiens (human) | 10082 | GPC6 |
|
||
| DOID:7148 | rheumatoid arthritis | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
|
||
| DOID:0110658 | congenital myasthenic syndrome 15 | HGNC:28287 | Homo sapiens (human) | 199857 | ALG14 |
|
||
| DOID:0111633 | congenital sucrase-isomaltase deficiency | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
|
||
| DOID:0060917 | facioscapulohumeral muscular dystrophy 3 | HGNC:30299 | Homo sapiens (human) | 55791 | LRIF1 |
|
||
| DOID:0111029 | hemochromatosis type 1 | HGNC:1069 | Homo sapiens (human) | 650 | BMP2 |
|
||
| DOID:0050902 | medulloblastoma | HGNC:9586 | Homo sapiens (human) | 8643 | PTCH2 |
|
