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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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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:9970 | obesity | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0080746 | Sweet syndrome | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:1245 | vulva cancer | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:3132 | porphyria cutanea tarda | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:10123 | pigmentation disease | HGNC:12450 | Homo sapiens (human) | 7306 | TYRP1 |
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| DOID:14701 | propionic acidemia | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0112359 | congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay | HGNC:11183 | Homo sapiens (human) | 6651 | SON |
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| DOID:0060685 | autosomal dominant nocturnal frontal lobe epilepsy 4 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:9675 | pulmonary emphysema | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:0110146 | Bartter disease type 4b | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:13533 | osteopetrosis | HGNC:29017 | Homo sapiens (human) | 9842 | PLEKHM1 |
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| DOID:10123 | pigmentation disease | HGNC:6929 | Homo sapiens (human) | 4157 | MC1R |
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| DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:824 | periodontitis | HGNC:3309 | Homo sapiens (human) | 1991 | ELANE |
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| DOID:1993 | rectum cancer | HGNC:7230 | Homo sapiens (human) | 4361 | MRE11 |
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| DOID:0080330 | cold-induced sweating syndrome 2 | HGNC:17412 | Homo sapiens (human) | 23529 | CLCF1 |
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| DOID:0050902 | medulloblastoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:3144 | cutis laxa | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:3008 | invasive ductal carcinoma | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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| DOID:1059 | intellectual disability | HGNC:18683 | Homo sapiens (human) | 9775 | EIF4A3 |
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| DOID:5844 | myocardial infarction | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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