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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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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:0110180 | Charcot-Marie-Tooth disease axonal type 2CC | HGNC:7737 | Homo sapiens (human) | 4744 | NEFH |
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| DOID:0080294 | Charcot-Marie-Tooth disease dominant intermediate G | HGNC:7739 | Homo sapiens (human) | 4747 | NEFL |
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| DOID:0081366 | Paget's disease of bone 3 | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:0050877 | pancreatic agenesis | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0081352 | congenital myopathy 20 | HGNC:10485 | Homo sapiens (human) | 6263 | RYR3 |
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| DOID:0080538 | Sweeney-Cox syndrome | HGNC:12428 | Homo sapiens (human) | 7291 | TWIST1 |
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| DOID:0110056 | amelogenesis imperfecta type 1C | HGNC:3344 | Homo sapiens (human) | 10117 | ENAM |
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| DOID:5419 | schizophrenia | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:0110219 | Brugada syndrome 2 | HGNC:28956 | Homo sapiens (human) | 23171 | GPD1L |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:11018 | Homo sapiens (human) | 140679 | SLC32A1 |
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| DOID:0112222 | developmental and epileptic encephalopathy 88 | HGNC:6970 | Homo sapiens (human) | 4190 | MDH1 |
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| DOID:0070459 | hereditary spastic paraplegia 90A | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:399 | tuberculosis | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0110225 | Brugada syndrome 8 | HGNC:16882 | Homo sapiens (human) | 10021 | HCN4 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4124 | Homo sapiens (human) | 2590 | GALNT2 |
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| DOID:0111641 | autosomal recessive nonsyndromic deafness 94 | HGNC:26274 | Homo sapiens (human) | 79731 | NARS2 |
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| DOID:0112329 | pontocerebellar hypoplasia type 2F | HGNC:16791 | Homo sapiens (human) | 116461 | TSEN15 |
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| DOID:0111547 | retinal arterial tortuosity | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:0081145 | common variable immunodeficiency 2 | HGNC:18153 | Homo sapiens (human) | 23495 | TNFRSF13B |
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| DOID:0111967 | immunodeficiency 54 | HGNC:6947 | Homo sapiens (human) | 4173 | MCM4 |
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| DOID:0112199 | spondyloepimetaphyseal dysplasia with joint laxity type 2 | HGNC:6391 | Homo sapiens (human) | 3835 | KIF22 |
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| DOID:0050591 | tooth agenesis | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:0112187 | thyroid dyshormonogenesis 3 | HGNC:11764 | Homo sapiens (human) | 7038 | TG |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:15840 | Homo sapiens (human) | 9757 | KMT2B |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:31042 | Homo sapiens (human) | 80000 | GREB1L |
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