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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:0080384 | nephrotic syndrome type 6 | HGNC:9678 | Homo sapiens (human) | 5800 | PTPRO |
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| DOID:0081020 | congenital fibrosis of the extraocular muscles 5 | HGNC:18603 | Homo sapiens (human) | 84570 | COL25A1 |
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| DOID:11830 | myopia | HGNC:20502 | Homo sapiens (human) | 283375 | SLC39A5 |
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| DOID:0080962 | anauxetic dysplasia 2 | HGNC:30129 | Homo sapiens (human) | 10940 | POP1 |
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| DOID:0070316 | Miura type epiphyseal chondrodysplasia | HGNC:7944 | Homo sapiens (human) | 4882 | NPR2 |
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| DOID:0111578 | Gillespie syndrome | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:0112214 | developmental and epileptic encephalopathy 78 | HGNC:4076 | Homo sapiens (human) | 2555 | GABRA2 |
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| DOID:0110433 | dilated cardiomyopathy 1E | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0081358 | epidermolytic hyperkeratosis 1 | HGNC:6412 | Homo sapiens (human) | 3848 | KRT1 |
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| DOID:0070277 | primary autosomal recessive microcephaly 15 | HGNC:25897 | Homo sapiens (human) | 84879 | MFSD2A |
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| DOID:0080318 | megalencephalic leukoencephalopathy with subcortical cysts 2A | HGNC:26361 | Homo sapiens (human) | 220296 | HEPACAM |
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| DOID:0111546 | Currarino syndrome | HGNC:4979 | Homo sapiens (human) | 3110 | MNX1 |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0111384 | inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 | HGNC:5033 | Homo sapiens (human) | 3181 | HNRNPA2B1 |
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| DOID:0110759 | type 1 diabetes mellitus 22 | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0111492 | combined oxidative phosphorylation deficiency 32 | HGNC:16618 | Homo sapiens (human) | 65993 | MRPS34 |
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| DOID:0060774 | congenital diarrhea | HGNC:16526 | Homo sapiens (human) | 51703 | ACSL5 |
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| DOID:0111425 | restrictive cardiomyopathy 1 | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:0080381 | nephrotic syndrome type 13 | HGNC:18658 | Homo sapiens (human) | 23165 | NUP205 |
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| DOID:9620 | vesicoureteral reflux | HGNC:10250 | Homo sapiens (human) | 6092 | ROBO2 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:6278 | Homo sapiens (human) | 3777 | KCNK3 |
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| DOID:0111636 | autosomal recessive nonsyndromic deafness 113 | HGNC:31948 | Homo sapiens (human) | 388551 | CEACAM16 |
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| DOID:0111579 | asthma, nasal polyps, and aspirin intolerance | HGNC:9594 | Homo sapiens (human) | 5732 | PTGER2 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:7590 | Homo sapiens (human) | 4638 | MYLK |
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