Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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:0110721 | neuronal ceroid lipofuscinosis 1 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
|
||
| DOID:0110728 | neuronal ceroid lipofuscinosis 5 | MGI:2442253 | Mus musculus (house mouse) | 211286 | Cln5 |
|
||
| DOID:0110728 | neuronal ceroid lipofuscinosis 5 | HGNC:2076 | Homo sapiens (human) | 1203 | CLN5 |
|
||
| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
|
||
| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:7694 | Homo sapiens (human) | 4706 | NDUFAB1 |
|
||
| DOID:0110735 | neurodegeneration with brain iron accumulation 2a | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
|
||
| DOID:0110736 | neurodegeneration with brain iron accumulation 2b | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | MGI:96572 | Mus musculus (house mouse) | 16333 | Ins1 |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | Xenbase:XB-GENE-6252363 | Xenopus laevis (African clawed frog) | 378696 | ins.S |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | Xenbase:XB-GENE-864803 | Xenopus laevis (African clawed frog) | 378695 | ins.L |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | RGD:2916 | Rattus norvegicus (Norway rat) | 24506 | Ins2 |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | MGI:1315197 | Mus musculus (house mouse) | 15277 | Hk2 |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | RGD:2915 | Rattus norvegicus (Norway rat) | 24505 | Ins1 |
|
||
| DOID:0110741 | type 1 diabetes mellitus 2 | ZFIN:ZDB-GENE-980526-110 | Danio rerio (zebrafish) | 30262 | ins |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | ZFIN:ZDB-GENE-100728-3 | Danio rerio (zebrafish) | 793635 | b4galnt1b |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | Xenbase:XB-GENE-17345437 | Xenopus laevis (African clawed frog) | 108709867 | b4galnt1.S |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | ZFIN:ZDB-GENE-070112-1462 | Danio rerio (zebrafish) | 558684 | b4galnt1a |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | MGI:1342057 | Mus musculus (house mouse) | 14421 | B4galnt1 |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | Xenbase:XB-GENE-960512 | Xenopus tropicalis (tropical clawed frog) | 100145208 | b4galnt1 |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | Xenbase:XB-GENE-960515 | Xenopus laevis (African clawed frog) | 379299 | b4galnt1.L |
|
||
| DOID:0110777 | hereditary spastic paraplegia 26 | RGD:620490 | Rattus norvegicus (Norway rat) | 64828 | B4galnt1 |
|
||
| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
|
