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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:0112248 | 17-beta hydroxysteroid dehydrogenase 3 deficiency | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | HGNC:2074 | Homo sapiens (human) | 1201 | CLN3 |
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| DOID:3070 | high grade glioma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0050436 | mulibrey nanism | HGNC:7523 | Homo sapiens (human) | 4591 | TRIM37 |
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| DOID:0110721 | neuronal ceroid lipofuscinosis 1 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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| DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:0080409 | familial adenomatous polyposis 1 | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:0081265 | intellectual developmental disorder with abnormal behavior, microcephaly, and short stature | HGNC:26033 | Homo sapiens (human) | 54517 | PUS7 |
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| DOID:0060285 | parietal foramina | HGNC:450 | Homo sapiens (human) | 60529 | ALX4 |
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| DOID:0110159 | Charcot-Marie-Tooth disease type 2B | HGNC:9788 | Homo sapiens (human) | 7879 | RAB7A |
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| DOID:0110913 | adult hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0111190 | distal myopathy 4 | HGNC:3756 | Homo sapiens (human) | 2318 | FLNC |
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| DOID:0060296 | congenital secretory chloride diarrhea 1 | HGNC:3018 | Homo sapiens (human) | 1811 | SLC26A3 |
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| DOID:0111066 | congenital bile acid synthesis defect 5 | HGNC:67 | Homo sapiens (human) | 5825 | ABCD3 |
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| DOID:0112224 | chondrodysplasia with joint dislocations gPAPP type | HGNC:26019 | Homo sapiens (human) | 54928 | BPNT2 |
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| DOID:0110403 | retinitis pigmentosa 13 | HGNC:17340 | Homo sapiens (human) | 10594 | PRPF8 |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:2910 | Homo sapiens (human) | 54567 | DLL4 |
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| DOID:0060488 | Pitt-Hopkins syndrome | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
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| DOID:0111590 | Cohen syndrome | HGNC:2183 | Homo sapiens (human) | 157680 | VPS13B |
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| DOID:0110832 | Usher syndrome type 1F | HGNC:14674 | Homo sapiens (human) | 65217 | PCDH15 |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
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| DOID:0050752 | amyotrophic lateral sclerosis type 8 | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:7569 | Homo sapiens (human) | 4629 | MYH11 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:1060 | Hartnup disease | HGNC:27960 | Homo sapiens (human) | 340024 | SLC6A19 |
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