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 / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
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:8947 | diabetic retinopathy | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
|
||
| DOID:2723 | dermatitis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
|
||
| DOID:0110542 | autosomal dominant nonsyndromic deafness 10 | HGNC:3522 | Homo sapiens (human) | 2070 | EYA4 |
|
||
| DOID:9352 | type 2 diabetes mellitus | RGD:1308135 | Rattus norvegicus (Norway rat) | 361722 | Bscl2 |
|
||
| DOID:1324 | lung cancer | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
|
||
| DOID:0070114 | Niemann-Pick disease type C2 | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
|
||
| DOID:9538 | multiple myeloma | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
|
||
| DOID:13810 | familial hypercholesterolemia | HGNC:603 | Homo sapiens (human) | 338 | APOB |
|
||
| DOID:1287 | cardiovascular system disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
|
||
| DOID:0081146 | common variable immunodeficiency 3 | HGNC:1633 | Homo sapiens (human) | 930 | CD19 |
|
||
| DOID:0090136 | complex cortical dysplasia with other brain malformations 6 | HGNC:20778 | Homo sapiens (human) | 203068 | TUBB |
|
||
| DOID:13544 | low tension glaucoma | HGNC:613 | Homo sapiens (human) | 348 | APOE |
|
||
| DOID:0081119 | benign familial infantile seizures 6 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
|
||
| DOID:0060848 | developmental and epileptic encephalopathy 9 | HGNC:14270 | Homo sapiens (human) | 57526 | PCDH19 |
|
||
| DOID:4586 | familial meningioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
|
||
| DOID:11394 | adult respiratory distress syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
|
||
| DOID:10825 | essential hypertension | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
|
||
| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
|
||
| DOID:0111730 | familial episodic pain syndrome 2 | HGNC:10582 | Homo sapiens (human) | 6336 | SCN10A |
|
||
| DOID:1962 | fallopian tube disease | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
|
||
| DOID:11713 | diabetic angiopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0060669 | cerebral cavernous malformation | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
|
||
| DOID:9744 | type 1 diabetes mellitus | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
|
||
| DOID:0050591 | tooth agenesis | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
|
||
| DOID:3526 | cerebral infarction | HGNC:9456 | Homo sapiens (human) | 5627 | PROS1 |
|
