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:0060884 | renal hypomagnesemia 6 | HGNC:103 | Homo sapiens (human) | 54805 | CNNM2 |
|
||
| DOID:0111351 | D-2-hydroxyglutaric aciduria 1 | HGNC:28358 | Homo sapiens (human) | 728294 | D2HGDH |
|
||
| DOID:0060892 | late onset Parkinson's disease | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
|
||
| DOID:0110163 | Charcot-Marie-Tooth disease axonal type 2F | HGNC:5246 | Homo sapiens (human) | 3315 | HSPB1 |
|
||
| DOID:0070380 | developmental and epileptic encephalopathy 85 | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
|
||
| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
|
||
| DOID:0112307 | sarcosinemia | HGNC:10536 | Homo sapiens (human) | 1757 | SARDH |
|
||
| DOID:0090086 | hypogonadotropic hypogonadism 6 with or without anosmia | HGNC:3686 | Homo sapiens (human) | 2253 | FGF8 |
|
||
| DOID:0060575 | 3MC syndrome 1 | HGNC:6901 | Homo sapiens (human) | 5648 | MASP1 |
|
||
| DOID:0081363 | distal myopathy with rimmed vacuoles | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
|
||
| DOID:0111358 | Floating-Harbor syndrome | HGNC:16974 | Homo sapiens (human) | 10847 | SRCAP |
|
||
| DOID:0081325 | developmental and epileptic encephalopathy 94 | HGNC:1917 | Homo sapiens (human) | 1106 | CHD2 |
|
||
| DOID:0070274 | hereditary nonpolyposis colorectal cancer type 2 | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
|
||
| DOID:0110920 | hereditary spherocytosis type 5 | HGNC:3381 | Homo sapiens (human) | 2038 | EPB42 |
|
||
| DOID:0070302 | multiple epiphyseal dysplasia 7 | HGNC:19721 | Homo sapiens (human) | 124583 | CANT1 |
|
||
| DOID:0110965 | brachydactyly type A2 | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
|
||
| DOID:0070511 | polyhydramnios, megalencephaly, and symptomatic epilepsy | HGNC:30172 | Homo sapiens (human) | 92335 | STRADA |
|
||
| DOID:0110338 | osteogenesis imperfecta type 17 | HGNC:11219 | Homo sapiens (human) | 6678 | SPARC |
|
||
| DOID:0111227 | frontotemporal dementia and/or amyotrophic lateral sclerosis 7 | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
|
||
| DOID:612 | primary immunodeficiency disease | HGNC:11408 | Homo sapiens (human) | 6789 | STK4 |
|
||
| DOID:9253 | gastrointestinal stromal tumor | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
|
||
| DOID:0060491 | SPOAN syndrome | HGNC:20716 | Homo sapiens (human) | 64837 | KLC2 |
|
||
| DOID:0070246 | X-linked Emery-Dreifuss muscular dystrophy 1 | HGNC:3331 | Homo sapiens (human) | 2010 | EMD |
|
||
| DOID:0050592 | asphyxiating thoracic dystrophy | HGNC:29239 | Homo sapiens (human) | 27152 | INTU |
|
||
| DOID:2340 | craniosynostosis | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
|
