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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
LM-GlycoRepo
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:3571 | liver cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:11446 | sciatic neuropathy | HGNC:14076 | Homo sapiens (human) | 29956 | CERS2 |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:5679 | retinal disease | HGNC:24289 | Homo sapiens (human) | 10390 | CEPT1 |
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| DOID:0080142 | mosaic variegated aneuploidy syndrome 2 | HGNC:30794 | Homo sapiens (human) | 9702 | CEP57 |
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| DOID:0110984 | Joubert syndrome 15 | HGNC:12370 | Homo sapiens (human) | 95681 | CEP41 |
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| DOID:0111123 | nephronophthisis 15 | HGNC:29182 | Homo sapiens (human) | 22897 | CEP164 |
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| DOID:684 | hepatocellular carcinoma | HGNC:29182 | Homo sapiens (human) | 22897 | CEP164 |
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| DOID:0070012 | Seckel syndrome 5 | HGNC:29298 | Homo sapiens (human) | 22995 | CEP152 |
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| DOID:0070292 | primary autosomal recessive microcephaly 9 | HGNC:29298 | Homo sapiens (human) | 22995 | CEP152 |
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| DOID:0070282 | primary autosomal recessive microcephaly 8 | HGNC:29086 | Homo sapiens (human) | 9662 | CEP135 |
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| DOID:1935 | Bardet-Biedl syndrome | HGNC:29511 | Homo sapiens (human) | 22994 | CEP131 |
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| DOID:0110994 | Joubert syndrome 25 | HGNC:24866 | Homo sapiens (human) | 9731 | CEP104 |
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| DOID:0081236 | autosomal recessive intellectual developmental disorder 77 | HGNC:24866 | Homo sapiens (human) | 9731 | CEP104 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:1857 | Homo sapiens (human) | 1063 | CENPF |
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| DOID:0110595 | Stromme syndrome | HGNC:1857 | Homo sapiens (human) | 1063 | CENPF |
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| DOID:0070283 | primary autosomal recessive microcephaly 13 | HGNC:1856 | Homo sapiens (human) | 1062 | CENPE |
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| DOID:0060218 | CREST syndrome | HGNC:1854 | Homo sapiens (human) | 1060 | CENPC |
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| DOID:5082 | liver cirrhosis | HGNC:1854 | Homo sapiens (human) | 1060 | CENPC |
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| DOID:10908 | hydrocephalus | HGNC:3231 | Homo sapiens (human) | 1952 | CELSR2 |
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| DOID:0050580 | hereditary lymphedema | HGNC:1850 | Homo sapiens (human) | 9620 | CELSR1 |
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| DOID:0070383 | developmental and epileptic encephalopathy 97 | HGNC:2550 | Homo sapiens (human) | 10659 | CELF2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:3153 | lipomatosis | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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