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:0090041 | torsion dystonia 4 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
|
||
| DOID:0070168 | spermatogenic failure 3 | HGNC:14468 | Homo sapiens (human) | 116369 | SLC26A8 |
|
||
| DOID:3393 | coronary artery disease | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
|
||
| DOID:3312 | bipolar disorder | HGNC:4585 | Homo sapiens (human) | 2903 | GRIN2A |
|
||
| DOID:0110838 | Usher syndrome type 2A | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
|
||
| DOID:0060023 | immunodeficiency with hyper IgM type 3 | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
|
||
| DOID:9008 | psoriatic arthritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
|
||
| DOID:0081319 | multiple synostoses syndrome 3 | HGNC:3687 | Homo sapiens (human) | 2254 | FGF9 |
|
||
| DOID:4947 | cholangiocarcinoma | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
|
||
| DOID:0111346 | epidermolysis bullosa simplex with mottled pigmentation | HGNC:6442 | Homo sapiens (human) | 3852 | KRT5 |
|
||
| DOID:2154 | nephroblastoma | HGNC:9966 | Homo sapiens (human) | 5978 | REST |
|
||
| DOID:2377 | multiple sclerosis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
|
||
| DOID:0081109 | keratosis palmoplantaris striata 2 | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
|
||
| DOID:0060233 | cardiofaciocutaneous syndrome | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
|
||
| DOID:1067 | open-angle glaucoma | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
|
||
| DOID:2043 | hepatitis B | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
|
||
| DOID:0080860 | primary ovarian insufficiency 3 | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
|
||
| DOID:1024 | leprosy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:10629 | microphthalmia | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
|
||
| DOID:10534 | stomach cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
|
||
| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
|
||
| DOID:0110856 | posterior polymorphous corneal dystrophy 2 | HGNC:2216 | Homo sapiens (human) | 1296 | COL8A2 |
|
||
| DOID:9970 | obesity | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
|
||
| DOID:0080074 | neural tube defect | HGNC:26219 | Homo sapiens (human) | 80199 | FUZ |
|
