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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:2750 | glycogen storage disease IV | MGI:1921435 | Mus musculus (house mouse) | 74185 | Gbe1 |
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| DOID:0060900 | Parkinson's disease 14 | MGI:1859152 | Mus musculus (house mouse) | 53357 | Pla2g6 |
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| DOID:0070151 | hereditary sensory and autonomic neuropathy type 6 | MGI:104627 | Mus musculus (house mouse) | 13518 | Dst |
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| DOID:0050787 | juvenile polyposis syndrome | MGI:1338938 | Mus musculus (house mouse) | 12166 | Bmpr1a |
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| DOID:0111403 | mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations | MGI:1861901 | Mus musculus (house mouse) | 56527 | Mast1 |
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| DOID:0060866 | patterned macular dystrophy 1 | MGI:102791 | Mus musculus (house mouse) | 19133 | Prph2 |
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| DOID:0050477 | Liddle syndrome | MGI:104696 | Mus musculus (house mouse) | 20277 | Scnn1b |
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| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | MGI:96257 | Mus musculus (house mouse) | 15530 | Hspg2 |
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| DOID:0111138 | congenital generalized lipodystrophy type 4 | MGI:1277968 | Mus musculus (house mouse) | 19285 | Cavin1 |
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| DOID:0110144 | Bartter disease type 3 | MGI:1930643 | Mus musculus (house mouse) | 56365 | Clcnkb |
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| DOID:0110475 | autosomal recessive nonsyndromic deafness 1A | MGI:107588 | Mus musculus (house mouse) | 14623 | Gjb6 |
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| DOID:0110877 | holoprosencephaly 11 | MGI:1926387 | Mus musculus (house mouse) | 57810 | Cdon |
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| DOID:0110766 | hereditary spastic paraplegia 13 | MGI:96242 | Mus musculus (house mouse) | 15510 | Hspd1 |
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| DOID:3827 | congenital diaphragmatic hernia | MGI:1315202 | Mus musculus (house mouse) | 20564 | Slit3 |
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| DOID:0060733 | junctional epidermolysis bullosa with pyloric atresia | MGI:96613 | Mus musculus (house mouse) | 192897 | Itgb4 |
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| DOID:9970 | obesity | MGI:96929 | Mus musculus (house mouse) | 17201 | Mc3r |
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| DOID:0050816 | urofacial syndrome | MGI:2685814 | Mus musculus (house mouse) | 545291 | Hpse2 |
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| DOID:0110052 | amelogenesis imperfecta type 1B | MGI:1333772 | Mus musculus (house mouse) | 13801 | Enam |
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| DOID:0060798 | hypomyelinating leukodystrophy 6 | MGI:107848 | Mus musculus (house mouse) | 22153 | Tubb4a |
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| DOID:10140 | dry eye syndrome | MGI:104697 | Mus musculus (house mouse) | 17833 | Muc5ac |
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| DOID:2231 | factor XII deficiency | MGI:1891012 | Mus musculus (house mouse) | 58992 | F12 |
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| DOID:0090034 | myoclonic dystonia 11 | MGI:1329042 | Mus musculus (house mouse) | 20392 | Sgce |
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| DOID:2217 | Bernard-Soulier syndrome | MGI:107852 | Mus musculus (house mouse) | 14724 | Gp1bb |
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| DOID:1270 | hereditary hemorrhagic telangiectasia | MGI:1338946 | Mus musculus (house mouse) | 11482 | Acvrl1 |
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| DOID:0110953 | Waardenburg syndrome type 4A | MGI:102720 | Mus musculus (house mouse) | 13618 | Ednrb |
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