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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:631 | fibromyalgia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:10591 | pre-eclampsia | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:6713 | cerebrovascular disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0110267 | cataract 44 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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| DOID:5419 | schizophrenia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0080560 | congenital disorder of glycosylation Ih | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:11054 | urinary bladder cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:219 | colon cancer | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:3594 | choriocarcinoma | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:3454 | brain infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:13948 | bladder neck obstruction | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:5381 | bile duct adenoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:1407 | anterior uveitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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