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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
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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:2043 | hepatitis B | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:7873 | Homo sapiens (human) | 4843 | NOS2 |
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| DOID:0081231 | autosomal recessive intellectual developmental disorder 70 | HGNC:24152 | Homo sapiens (human) | 51319 | RSRC1 |
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| DOID:1682 | congenital heart disease | HGNC:7775 | Homo sapiens (human) | 4772 | NFATC1 |
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| DOID:9415 | allergic asthma | HGNC:4938 | Homo sapiens (human) | 3113 | HLA-DPA1 |
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| DOID:10652 | Alzheimer's disease | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0050661 | vitelliform macular dystrophy | HGNC:6055 | Homo sapiens (human) | 3617 | IMPG1 |
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| DOID:11396 | pulmonary edema | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:0050741 | alcohol dependence | HGNC:8153 | Homo sapiens (human) | 4985 | OPRD1 |
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| DOID:3393 | coronary artery disease | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:8501 | fundus dystrophy | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:8544 | chronic fatigue syndrome | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0050697 | chorioamnionitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0111278 | histiocytosis-lymphadenopathy plus syndrome | HGNC:23096 | Homo sapiens (human) | 55315 | SLC29A3 |
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| DOID:0080918 | polymicrogyria | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:0111643 | autosomal recessive nonsyndromic deafness 115 | HGNC:26992 | Homo sapiens (human) | 124976 | SPNS2 |
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| DOID:905 | Zellweger syndrome | HGNC:67 | Homo sapiens (human) | 5825 | ABCD3 |
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| DOID:4483 | rhinitis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:6039 | uveal melanoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:1580 | diffuse scleroderma | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:674 | cleft palate | HGNC:10257 | Homo sapiens (human) | 4920 | ROR2 |
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| DOID:0070300 | multiple epiphyseal dysplasia 4 | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0081218 | autosomal recessive intellectual developmental disorder 74 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:5844 | myocardial infarction | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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