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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:10286 | prostate carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:10591 | pre-eclampsia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:9538 | multiple myeloma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:418 | systemic scleroderma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:13375 | temporal arteritis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:2841 | asthma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:5844 | myocardial infarction | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:1380 | endometrial cancer | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:3371 | chondrosarcoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:1826 | epilepsy | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:224 | transient cerebral ischemia | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:219 | colon cancer | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:10907 | microcephaly | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:0050912 | colon adenoma | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:8619 | recurrent hypersomnia | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:9884 | muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:10907 | microcephaly | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:1059 | intellectual disability | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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