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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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 | October 9, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060404 | chromosome 17q12 deletion syndrome | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | HGNC:17007 | Homo sapiens (human) | 11072 | DUSP14 |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | MGI:108451 | Mus musculus (house mouse) | 107476 | Acaca |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | HGNC:19235 | Homo sapiens (human) | 26574 | AATF |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | MGI:2140940 | Mus musculus (house mouse) | 100705 | Acacb |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | SGD:S000004820 | Saccharomyces cerevisiae S288C | 855247 | HFA1 |
|
||
| DOID:0060399 | chromosome 16p12.1 deletion syndrome | RGD:1359150 | Rattus norvegicus (Norway rat) | 293448 | Uqcrc2 |
|
||
| DOID:0060399 | chromosome 16p12.1 deletion syndrome | HGNC:30347 | Homo sapiens (human) | 55718 | POLR3E |
|
||
| DOID:0060399 | chromosome 16p12.1 deletion syndrome | HGNC:12586 | Homo sapiens (human) | 7385 | UQCRC2 |
|
||
| DOID:0060399 | chromosome 16p12.1 deletion syndrome | HGNC:27087 | Homo sapiens (human) | 730094 | MOSMO |
|
||
| DOID:0060399 | chromosome 16p12.1 deletion syndrome | MGI:2446240 | Mus musculus (house mouse) | 233812 | Mosmo |
|
||
| DOID:0060399 | chromosome 16p12.1 deletion syndrome | MGI:1914253 | Mus musculus (house mouse) | 67003 | Uqcrc2 |
|
||
| DOID:0060398 | chromosome 16p11.2 deletion syndrome, 220-kb | HGNC:30417 | Homo sapiens (human) | 25970 | SH2B1 |
|
||
| DOID:0060395 | chromosome 15q24 deletion syndrome | HGNC:19353 | Homo sapiens (human) | 25942 | SIN3A |
|
||
| DOID:0060395 | chromosome 15q24 deletion syndrome | MGI:107157 | Mus musculus (house mouse) | 20466 | Sin3a |
|
||
| DOID:0060395 | chromosome 15q24 deletion syndrome | SGD:S000005364 | Saccharomyces cerevisiae S288C | 854158 | SIN3 |
|
||
| DOID:0060395 | chromosome 15q24 deletion syndrome | FB:FBgn0022764 | Drosophila melanogaster (fruit fly) | 36382 | Sin3A |
|
||
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | HGNC:7146 | Homo sapiens (human) | 4308 | TRPM1 |
|
||
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | HGNC:20718 | Homo sapiens (human) | 161725 | OTUD7A |
|
||
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | HGNC:17992 | Homo sapiens (human) | 80036 | TRPM3 |
|
||
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | HGNC:17995 | Homo sapiens (human) | 140803 | TRPM6 |
|
||
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | RGD:1597140 | Rattus norvegicus (Norway rat) | 361586 | Trpm1 |
|
||
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | MGI:1330305 | Mus musculus (house mouse) | 17364 | Trpm1 |
|
||
| DOID:0060393 | chromosome 15q11.2 deletion syndrome | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
|
