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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:14219 | renal tubular acidosis | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
|
||
| DOID:0110704 | hypotrichosis 7 | HGNC:18483 | Homo sapiens (human) | 200879 | LIPH |
|
||
| DOID:0050589 | inflammatory bowel disease | HGNC:18486 | Homo sapiens (human) | 23037 | PDZD2 |
|
||
| DOID:0050580 | hereditary lymphedema | HGNC:1850 | Homo sapiens (human) | 9620 | CELSR1 |
|
||
| DOID:0050155 | sensory system disease | HGNC:18502 | Homo sapiens (human) | 90665 | TBL1Y |
|
||
| DOID:0111758 | Y-linked deafness 2 | HGNC:18502 | Homo sapiens (human) | 90665 | TBL1Y |
|
||
| DOID:9778 | irritable bowel syndrome | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:10534 | stomach cancer | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:218 | ascending colon cancer | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:3717 | gastric adenocarcinoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:5517 | stomach carcinoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:9256 | colorectal cancer | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:4947 | cholangiocarcinoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:219 | colon cancer | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:3910 | lung adenocarcinoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:3070 | high grade glioma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:1380 | endometrial cancer | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:0050869 | villous adenoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
|
||
| DOID:0050886 | Troyer syndrome | HGNC:18514 | Homo sapiens (human) | 23111 | SPART |
|
||
| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:18533 | Homo sapiens (human) | 84196 | USP48 |
|
||
| DOID:0060218 | CREST syndrome | HGNC:1854 | Homo sapiens (human) | 1060 | CENPC |
|
||
| DOID:5082 | liver cirrhosis | HGNC:1854 | Homo sapiens (human) | 1060 | CENPC |
|
||
| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
|
