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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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:0110056 | amelogenesis imperfecta type 1C | HGNC:3344 | Homo sapiens (human) | 10117 | ENAM |
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| DOID:12185 | otosclerosis | HGNC:1069 | Homo sapiens (human) | 650 | BMP2 |
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| DOID:5419 | schizophrenia | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:13560 | subserous uterine fibroid | HGNC:29190 | Homo sapiens (human) | 23112 | TNRC6B |
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| DOID:8947 | diabetic retinopathy | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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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:0050741 | alcohol dependence | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:0112222 | developmental and epileptic encephalopathy 88 | HGNC:6970 | Homo sapiens (human) | 4190 | MDH1 |
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| DOID:11830 | myopia | HGNC:6482 | Homo sapiens (human) | 3908 | LAMA2 |
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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:12858 | Huntington's disease | HGNC:4586 | Homo sapiens (human) | 2904 | GRIN2B |
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| DOID:1059 | intellectual disability | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:1485 | cystic fibrosis | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:1407 | anterior uveitis | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0110225 | Brugada syndrome 8 | HGNC:16882 | Homo sapiens (human) | 10021 | HCN4 |
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| DOID:13241 | Behcet's disease | HGNC:4935 | Homo sapiens (human) | 3109 | HLA-DMB |
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| DOID:1059 | intellectual disability | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0050741 | alcohol dependence | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4124 | Homo sapiens (human) | 2590 | GALNT2 |
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| DOID:3883 | Lynch syndrome | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:1584 | acute chest syndrome | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:0111641 | autosomal recessive nonsyndromic deafness 94 | HGNC:26274 | Homo sapiens (human) | 79731 | NARS2 |
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| DOID:1793 | pancreatic cancer | HGNC:6140 | Homo sapiens (human) | 3676 | ITGA4 |
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