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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
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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:2590 | familial nephrotic syndrome | HGNC:6485 | Homo sapiens (human) | 3911 | LAMA5 |
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| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:14448 | 46,XY sex reversal | HGNC:17210 | Homo sapiens (human) | 57647 | DHX37 |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:4013 | Homo sapiens (human) | 2524 | FUT2 |
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| DOID:0110131 | Bardet-Biedl syndrome 9 | HGNC:30000 | Homo sapiens (human) | 27241 | BBS9 |
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| DOID:0070234 | Loeys-Dietz syndrome 2 | HGNC:11773 | Homo sapiens (human) | 7048 | TGFBR2 |
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| DOID:0060807 | syndromic X-linked intellectual disability Najm type | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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| DOID:0110440 | dilated cardiomyopathy 1J | HGNC:3522 | Homo sapiens (human) | 2070 | EYA4 |
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| DOID:0110681 | congenital myasthenic syndrome 2A | HGNC:1961 | Homo sapiens (human) | 1140 | CHRNB1 |
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| DOID:0110820 | hereditary spastic paraplegia 75 | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:0110098 | atopic dermatitis 2 | HGNC:3748 | Homo sapiens (human) | 2312 | FLG |
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| DOID:0090102 | autosomal dominant macrothrombocytopenia TUBB1-related | HGNC:16257 | Homo sapiens (human) | 81027 | TUBB1 |
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| DOID:0070139 | autosomal recessive cutis laxa type IC | HGNC:6717 | Homo sapiens (human) | 8425 | LTBP4 |
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| DOID:0111130 | focal segmental glomerulosclerosis 5 | HGNC:23791 | Homo sapiens (human) | 64423 | INF2 |
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| DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | HGNC:1152 | Homo sapiens (human) | 11149 | BVES |
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| DOID:14766 | renal agenesis | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:1349 | Homo sapiens (human) | 219285 | SAMD9L |
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| DOID:0080135 | multiple mitochondrial dysfunctions syndrome 3 | HGNC:27302 | Homo sapiens (human) | 200205 | IBA57 |
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| DOID:0060817 | syndromic X-linked intellectual disability 34 | HGNC:7871 | Homo sapiens (human) | 4841 | NONO |
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| DOID:0111955 | immunodeficiency 27A | HGNC:5439 | Homo sapiens (human) | 3459 | IFNGR1 |
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| DOID:4586 | familial meningioma | HGNC:7180 | Homo sapiens (human) | 4330 | MN1 |
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| DOID:0111228 | Sveinsson chorioretinal atrophy | HGNC:11714 | Homo sapiens (human) | 7003 | TEAD1 |
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| DOID:0111366 | familial hepatic adenoma | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:0111420 | familial GPIHBP1 deficiency | HGNC:24945 | Homo sapiens (human) | 338328 | GPIHBP1 |
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| DOID:0070354 | cataract 48 | HGNC:30373 | Homo sapiens (human) | 23268 | DNMBP |
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