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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
LM-GlycoRepo
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:14731 | Weaver syndrome | HGNC:3527 | Homo sapiens (human) | 2146 | EZH2 |
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| DOID:0060675 | catecholaminergic polymorphic ventricular tachycardia 1 | HGNC:10484 | Homo sapiens (human) | 6262 | RYR2 |
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| DOID:0050956 | spinocerebellar ataxia type 6 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0080097 | myofibrillar myopathy 6 | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:0060703 | Muenke Syndrome | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0111735 | X-linked deafness 4 | HGNC:11122 | Homo sapiens (human) | 23676 | SMPX |
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| DOID:0110431 | dilated cardiomyopathy 1I | HGNC:2770 | Homo sapiens (human) | 1674 | DES |
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| DOID:0111013 | cone-rod dystrophy 3 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:9256 | colorectal cancer | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:0110224 | Brugada syndrome 7 | HGNC:20665 | Homo sapiens (human) | 55800 | SCN3B |
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| DOID:0110865 | congenital stationary night blindness 1B | HGNC:4598 | Homo sapiens (human) | 2916 | GRM6 |
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| DOID:0111717 | isolated cryptophthalmia | HGNC:25396 | Homo sapiens (human) | 341640 | FREM2 |
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| DOID:11870 | Pick's disease | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:19721 | Homo sapiens (human) | 124583 | CANT1 |
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| DOID:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0111046 | platelet-type bleeding disorder 10 | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:0110210 | Charcot-Marie-Tooth disease X-linked recessive 5 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0110821 | hereditary spastic paraplegia 76 | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:0110423 | dilated cardiomyopathy 1C | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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| DOID:11713 | diabetic angiopathy | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:0110425 | dilated cardiomyopathy 1A | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0110722 | neuronal ceroid lipofuscinosis 7 | HGNC:28486 | Homo sapiens (human) | 256471 | MFSD8 |
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| DOID:0111671 | primary hyperoxaluria type 2 | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:0110768 | hereditary spastic paraplegia 15 | HGNC:20761 | Homo sapiens (human) | 23503 | ZFYVE26 |
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| DOID:0090142 | cystathioninuria | HGNC:2501 | Homo sapiens (human) | 1491 | CTH |
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