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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:0080131 | mitochondrial DNA depletion syndrome 13 | HGNC:13601 | Homo sapiens (human) | 26235 | FBXL4 |
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| DOID:0110447 | dilated cardiomyopathy 1DD | HGNC:27424 | Homo sapiens (human) | 282996 | RBM20 |
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| DOID:0050771 | pheochromocytoma | HGNC:9967 | Homo sapiens (human) | 5979 | RET |
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| DOID:0080475 | psoriasis 2 | HGNC:16446 | Homo sapiens (human) | 79092 | CARD14 |
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| DOID:0060230 | basal ganglia calcification | HGNC:10947 | Homo sapiens (human) | 6575 | SLC20A2 |
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| DOID:0112232 | lissencephaly 3 | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0050461 | aspartylglucosaminuria | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:0060205 | frontotemporal dementia and/or amyotrophic lateral sclerosis 6 | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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| DOID:0081271 | Smith-McCort dysplasia 2 | HGNC:16075 | Homo sapiens (human) | 83452 | RAB33B |
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| DOID:0080462 | developmental and epileptic encephalopathy 7 | HGNC:6296 | Homo sapiens (human) | 3785 | KCNQ2 |
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| DOID:0110864 | congenital stationary night blindness 1F | HGNC:24783 | Homo sapiens (human) | 345193 | LRIT3 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:0060650 | dicarboxylic aminoaciduria | HGNC:10939 | Homo sapiens (human) | 6505 | SLC1A1 |
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| DOID:0081272 | Sandestig-Stefanova syndrome | HGNC:17859 | Homo sapiens (human) | 23511 | NUP188 |
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| DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:0050545 | visceral heterotaxy | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:0111471 | combined oxidative phosphorylation deficiency 30 | HGNC:26022 | Homo sapiens (human) | 54931 | TRMT10C |
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| DOID:1612 | breast cancer | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:0050545 | visceral heterotaxy | HGNC:174 | Homo sapiens (human) | 93 | ACVR2B |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:33939 | Homo sapiens (human) | 645104 | CLRN2 |
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| DOID:0110358 | retinitis pigmentosa 12 | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:0080089 | tubular aggregate myopathy 1 | HGNC:11386 | Homo sapiens (human) | 6786 | STIM1 |
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| DOID:1933 | Rubinstein-Taybi syndrome | HGNC:2348 | Homo sapiens (human) | 1387 | CREBBP |
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