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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:4450 | renal cell carcinoma | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:0112151 | corpus callosum agenesis-abnormal genitalia syndrome | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0110441 | dilated cardiomyopathy 2B | HGNC:29941 | Homo sapiens (human) | 57798 | GATAD1 |
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| DOID:0080206 | CAKUT1 | HGNC:29043 | Homo sapiens (human) | 25778 | DSTYK |
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| DOID:783 | end stage renal disease | HGNC:2622 | Homo sapiens (human) | 1558 | CYP2C8 |
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| DOID:0080471 | developmental and epileptic encephalopathy 92 | HGNC:4082 | Homo sapiens (human) | 2561 | GABRB2 |
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| DOID:3312 | bipolar disorder | HGNC:4077 | Homo sapiens (human) | 2556 | GABRA3 |
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| DOID:0080985 | syndromic X-linked intellectual disorder Lujan-Fryns-type | HGNC:11957 | Homo sapiens (human) | 9968 | MED12 |
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| DOID:0110451 | dilated cardiomyopathy 1O | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:0111694 | familial adult myoclonic epilepsy 7 | HGNC:16854 | Homo sapiens (human) | 9693 | RAPGEF2 |
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| DOID:3770 | pulmonary fibrosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0110581 | autosomal dominant nonsyndromic deafness 56 | HGNC:5318 | Homo sapiens (human) | 3371 | TNC |
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| DOID:8970 | subacute sclerosing panencephalitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10579 | leukodystrophy | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:0070456 | hereditary spastic paraplegia 87 | HGNC:23787 | Homo sapiens (human) | 57156 | TMEM63C |
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| DOID:936 | brain disease | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:7148 | rheumatoid arthritis | HGNC:18171 | Homo sapiens (human) | 51744 | CD244 |
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| DOID:11249 | vitamin K deficiency bleeding | HGNC:4247 | Homo sapiens (human) | 2677 | GGCX |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0080074 | neural tube defect | HGNC:7432 | Homo sapiens (human) | 4522 | MTHFD1 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0111348 | multiple epiphyseal dysplasia with myopia and deafness | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:1612 | breast cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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