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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:0110436 | dilated cardiomyopathy 1L | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:0060001 | withdrawal disorder | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:14320 | generalized anxiety disorder | HGNC:5287 | Homo sapiens (human) | 3351 | HTR1B |
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| DOID:0080141 | mosaic variegated aneuploidy syndrome 1 | HGNC:1149 | Homo sapiens (human) | 701 | BUB1B |
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| DOID:0090145 | dopamine beta-hydroxylase deficiency | HGNC:2689 | Homo sapiens (human) | 1621 | DBH |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | HGNC:245 | Homo sapiens (human) | 120 | ADD3 |
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| DOID:2717 | Bloom syndrome | HGNC:1058 | Homo sapiens (human) | 641 | BLM |
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| DOID:0080026 | otospondylomegaepiphyseal dysplasia, autosomal recessive | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
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| DOID:10159 | osteonecrosis | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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| DOID:0060649 | congenital hereditary endothelial dystrophy of cornea | HGNC:16438 | Homo sapiens (human) | 83959 | SLC4A11 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:684 | hepatocellular carcinoma | RGD:3369 | Rattus norvegicus (Norway rat) | 25747 | Ppara |
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| DOID:0110456 | dilated cardiomyopathy 1R | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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| DOID:0110713 | Oguchi disease-2 | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | HGNC:9119 | Homo sapiens (human) | 9512 | PMPCB |
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| DOID:0090068 | giant axonal neuropathy 1 | HGNC:4137 | Homo sapiens (human) | 8139 | GAN |
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| DOID:0110939 | autosomal recessive osteopetrosis 5 | HGNC:21652 | Homo sapiens (human) | 28962 | OSTM1 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:0060798 | hypomyelinating leukodystrophy 6 | HGNC:20774 | Homo sapiens (human) | 10382 | TUBB4A |
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| DOID:0090031 | D-bifunctional protein deficiency | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:1078 | Homo sapiens (human) | 659 | BMPR2 |
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| DOID:0110430 | dilated cardiomyopathy 1G | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:12798 | mucopolysaccharidosis | HGNC:25239 | Homo sapiens (human) | 153642 | ARSK |
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| DOID:0110670 | congenital myasthenic syndrome 9 | HGNC:7525 | Homo sapiens (human) | 4593 | MUSK |
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