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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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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:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:0070242 | primary coenzyme Q10 deficiency 5 | HGNC:25302 | Homo sapiens (human) | 57017 | COQ9 |
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| DOID:0080345 | blepharocheilodontic syndrome 1 | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:0080456 | developmental and epileptic encephalopathy 46 | HGNC:4588 | Homo sapiens (human) | 2906 | GRIN2D |
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| DOID:0050477 | Liddle syndrome | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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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:0080471 | developmental and epileptic encephalopathy 92 | HGNC:4082 | Homo sapiens (human) | 2561 | GABRB2 |
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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:0110581 | autosomal dominant nonsyndromic deafness 56 | HGNC:5318 | Homo sapiens (human) | 3371 | TNC |
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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:0111348 | multiple epiphyseal dysplasia with myopia and deafness | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0110917 | hereditary spherocytosis type 2 | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:29673 | Homo sapiens (human) | 8076 | MFAP5 |
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| DOID:0080925 | cytochrome P450 oxidoreductase deficiency | HGNC:9208 | Homo sapiens (human) | 5447 | POR |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:9820 | Homo sapiens (human) | 5889 | RAD51C |
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| DOID:0081221 | autosomal recessive intellectual developmental disorder 59 | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:0111189 | distal myopathy 3 | HGNC:5031 | Homo sapiens (human) | 3178 | HNRNPA1 |
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| DOID:0070330 | multiple mitochondrial dysfunctions syndrome | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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