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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:0112346 | hereditary spastic paraplegia 83 | HGNC:28242 | Homo sapiens (human) | 84842 | HPDL |
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| DOID:1289 | neurodegenerative disease | HGNC:28242 | Homo sapiens (human) | 84842 | HPDL |
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| DOID:684 | hepatocellular carcinoma | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:4450 | renal cell carcinoma | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:224 | transient cerebral ischemia | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:1485 | cystic fibrosis | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:25896 | Homo sapiens (human) | 84876 | ORAI1 |
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| DOID:0080686 | tubular aggregate myopathy 2 | HGNC:25896 | Homo sapiens (human) | 84876 | ORAI1 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:25896 | Homo sapiens (human) | 84876 | ORAI1 |
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| DOID:0111976 | immunodeficiency 9 | HGNC:25896 | Homo sapiens (human) | 84876 | ORAI1 |
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| DOID:0070277 | primary autosomal recessive microcephaly 15 | HGNC:25897 | Homo sapiens (human) | 84879 | MFSD2A |
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| DOID:10907 | microcephaly | HGNC:25897 | Homo sapiens (human) | 84879 | MFSD2A |
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| DOID:612 | primary immunodeficiency disease | HGNC:30227 | Homo sapiens (human) | 84888 | SPPL2A |
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| DOID:9455 | lipid storage disease | HGNC:11061 | Homo sapiens (human) | 84889 | SLC7A3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:11061 | Homo sapiens (human) | 84889 | SLC7A3 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:1686 | glaucoma | HGNC:21205 | Homo sapiens (human) | 84894 | LINGO1 |
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| DOID:0081225 | autosomal recessive intellectual developmental disorder 64 | HGNC:21205 | Homo sapiens (human) | 84894 | LINGO1 |
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| DOID:0080581 | hyperekplexia 4 | HGNC:25903 | Homo sapiens (human) | 84896 | ATAD1 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
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| DOID:5082 | liver cirrhosis | HGNC:1983 | Homo sapiens (human) | 84916 | UTP4 |
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| DOID:12236 | primary biliary cholangitis | HGNC:1983 | Homo sapiens (human) | 84916 | UTP4 |
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| DOID:13580 | cholestasis | HGNC:1983 | Homo sapiens (human) | 84916 | UTP4 |
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