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GlyTouCan
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:0110077 | arrhythmogenic right ventricular dysplasia 9 | HGNC:9024 | Homo sapiens (human) | 5318 | PKP2 |
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| DOID:9256 | colorectal cancer | HGNC:1149 | Homo sapiens (human) | 701 | BUB1B |
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| DOID:0111068 | congenital bile acid synthesis defect 4 | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0080128 | mitochondrial DNA depletion syndrome 9 | HGNC:11449 | Homo sapiens (human) | 8802 | SUCLG1 |
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| DOID:0111158 | SADDAN | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | HGNC:4573 | Homo sapiens (human) | 2892 | GRIA3 |
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| DOID:1405 | primary angle-closure glaucoma | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:0081354 | congenital myopathy 22A | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0080299 | partial lipodystrophy | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0080081 | nonsyndromic congenital nail disorder 3 | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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| DOID:0080114 | mitochondrial complex III deficiency nuclear type 5 | HGNC:12586 | Homo sapiens (human) | 7385 | UQCRC2 |
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| DOID:0110972 | brachydactyly type E1 | HGNC:5136 | Homo sapiens (human) | 3239 | HOXD13 |
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| DOID:0110117 | autoimmune lymphoproliferative syndrome type 4 | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:612 | primary immunodeficiency disease | HGNC:9954 | Homo sapiens (human) | 5966 | REL |
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| DOID:13270 | erythropoietic protoporphyria | HGNC:2088 | Homo sapiens (human) | 10845 | CLPX |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:8766 | Homo sapiens (human) | 10015 | PDCD6IP |
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| DOID:0050778 | Meckel syndrome | HGNC:20652 | Homo sapiens (human) | 79770 | TXNDC15 |
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| DOID:0070279 | primary autosomal recessive microcephaly 14 | HGNC:25403 | Homo sapiens (human) | 163786 | SASS6 |
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| DOID:0070345 | vertebral anomalies and variable endocrine and T-cell dysfunction | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:0111842 | Keipert syndrome | HGNC:4452 | Homo sapiens (human) | 2239 | GPC4 |
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| DOID:0110709 | hypotrichosis 12 | HGNC:10313 | Homo sapiens (human) | 6144 | RPL21 |
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| DOID:0080788 | proximal symphalangism 2 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0081263 | neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities | HGNC:15717 | Homo sapiens (human) | 50628 | GEMIN4 |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:6254 | Homo sapiens (human) | 27133 | KCNH5 |
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| DOID:0110177 | Charcot-Marie-Tooth disease axonal type 2N | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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