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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:0050589 | inflammatory bowel disease | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0050741 | alcohol dependence | HGNC:4070 | Homo sapiens (human) | 2550 | GABBR1 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:6432 | pulmonary hypertension | HGNC:3374 | Homo sapiens (human) | 2034 | EPAS1 |
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| DOID:0060878 | hypoparathyroidism-deafness-renal disease syndrome | HGNC:4172 | Homo sapiens (human) | 2625 | GATA3 |
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| DOID:0070166 | spermatogenic failure 20 | HGNC:25631 | Homo sapiens (human) | 55779 | CFAP44 |
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| DOID:0050954 | spinocerebellar ataxia type 1 | HGNC:10548 | Homo sapiens (human) | 6310 | ATXN1 |
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| DOID:0060929 | non-syndromic X-linked intellectual developmental disorder 111 | HGNC:13449 | Homo sapiens (human) | 84631 | SLITRK2 |
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| DOID:0110841 | Usher syndrome type 3A | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:0060246 | MASA syndrome | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:0111395 | mucopolysaccharidosis type IIIA | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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| DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110633 | rigid spine muscular dystrophy 1 | HGNC:15999 | Homo sapiens (human) | 57190 | SELENON |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:0110424 | dilated cardiomyopathy 1CC | HGNC:29557 | Homo sapiens (human) | 91624 | NEXN |
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| DOID:3082 | interstitial lung disease | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:0110910 | leukocyte adhesion deficiency 1 | HGNC:6155 | Homo sapiens (human) | 3689 | ITGB2 |
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| DOID:0111611 | autosomal recessive spinocerebellar ataxia 4 | HGNC:23595 | Homo sapiens (human) | 55187 | VPS13D |
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| DOID:0110079 | Leber congenital amaurosis 8 | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:0111668 | Kohlschutter-Tonz syndrome | HGNC:29478 | Homo sapiens (human) | 79641 | ROGDI |
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| DOID:684 | hepatocellular carcinoma | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0050741 | alcohol dependence | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:1742 | drug psychosis | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0111030 | hemochromatosis type 3 | RGD:1310152 | Rattus norvegicus (Norway rat) | 288562 | Tfr2 |
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