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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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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:9256 | colorectal cancer | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:12387 | nephrogenic diabetes insipidus | HGNC:897 | Homo sapiens (human) | 554 | AVPR2 |
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| DOID:0110224 | Brugada syndrome 7 | HGNC:20665 | Homo sapiens (human) | 55800 | SCN3B |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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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:14323 | Marfan syndrome | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:11870 | Pick's disease | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:0111030 | hemochromatosis type 3 | RGD:1310152 | Rattus norvegicus (Norway rat) | 288562 | Tfr2 |
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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:594 | panic disorder | HGNC:5286 | Homo sapiens (human) | 3350 | HTR1A |
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| DOID:10763 | hypertension | HGNC:1029 | Homo sapiens (human) | 623 | BDKRB1 |
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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:12716 | newborn respiratory distress syndrome | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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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:9280 | carbamoyl phosphate synthetase I deficiency disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:0110722 | neuronal ceroid lipofuscinosis 7 | HGNC:28486 | Homo sapiens (human) | 256471 | MFSD8 |
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| DOID:12365 | malaria | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0060173 | Timothy syndrome | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0111671 | primary hyperoxaluria type 2 | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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