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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:10908 | hydrocephalus | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | ZFIN:ZDB-GENE-070103-2 | Danio rerio (zebrafish) | 791107 | hs6st1b |
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| DOID:0112136 | severe congenital neutropenia 4 | ZFIN:ZDB-GENE-061215-19 | Danio rerio (zebrafish) | 790919 | g6pc3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0080560 | congenital disorder of glycosylation Ih | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0050770 | polycystic liver disease | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:674 | cleft palate | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:3910 | lung adenocarcinoma | RGD:68346 | Rattus norvegicus (Norway rat) | 78959 | Akr1a1 |
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| DOID:1612 | breast cancer | RGD:68346 | Rattus norvegicus (Norway rat) | 78959 | Akr1a1 |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | RGD:69240 | Rattus norvegicus (Norway rat) | 78947 | Mogs |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | HGNC:24862 | Homo sapiens (human) | 7841 | MOGS |
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| DOID:0070395 | developmental and epileptic encephalopathy 110 | HGNC:1399 | Homo sapiens (human) | 781 | CACNA2D1 |
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| DOID:3454 | brain infarction | HGNC:1399 | Homo sapiens (human) | 781 | CACNA2D1 |
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| DOID:0060227 | Adams-Oliver syndrome | Xenbase:XB-GENE-994619 | Xenopus tropicalis (tropical clawed frog) | 780148 | eogt |
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| DOID:0080201 | Peters plus syndrome | Xenbase:XB-GENE-951583 | Xenopus tropicalis (tropical clawed frog) | 780006 | b3glct |
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| DOID:13276 | Mycoplasma pneumoniae pneumonia | Xenbase:XB-GENE-1000107 | Xenopus tropicalis (tropical clawed frog) | 779723 | galc |
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