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:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
|
||
| DOID:0090143 | brachyolmia-amelogenesis imperfecta syndrome | HGNC:6716 | Homo sapiens (human) | 4054 | LTBP3 |
|
||
| DOID:0050947 | hereditary hypophosphatemic rickets with hypercalciuria | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
|
||
| DOID:14261 | fragile X syndrome | HGNC:3775 | Homo sapiens (human) | 2332 | FMR1 |
|
||
| DOID:0080052 | acromesomelic dysplasia, Grebe type | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
|
||
| DOID:0080093 | myofibrillar myopathy 2 | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
|
||
| DOID:3755 | antithrombin III deficiency | HGNC:775 | Homo sapiens (human) | 462 | SERPINC1 |
|
||
| DOID:0111340 | dominant optic atrophy plus syndrome | HGNC:8140 | Homo sapiens (human) | 4976 | OPA1 |
|
||
| DOID:10159 | osteonecrosis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
|
||
| DOID:11476 | osteoporosis | HGNC:11926 | Homo sapiens (human) | 8600 | TNFSF11 |
|
||
| DOID:6432 | pulmonary hypertension | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
|
||
| DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
|
||
| DOID:0060895 | Parkinson's disease 4 | HGNC:11138 | Homo sapiens (human) | 6622 | SNCA |
|
||
| DOID:0060198 | amyotrophic lateral sclerosis type 6 | HGNC:4010 | Homo sapiens (human) | 2521 | FUS |
|
||
| DOID:14330 | Parkinson's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
|
||
| DOID:3827 | congenital diaphragmatic hernia | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
|
||
| DOID:0110859 | polycystic kidney disease 2 | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
|
||
| DOID:0111037 | glycine N-methyltransferase deficiency | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
|
||
| DOID:3883 | Lynch syndrome | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
|
||
| DOID:3770 | pulmonary fibrosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
|
||
| DOID:10581 | metachromatic leukodystrophy | HGNC:713 | Homo sapiens (human) | 410 | ARSA |
|
||
| DOID:9970 | obesity | HGNC:8743 | Homo sapiens (human) | 5122 | PCSK1 |
|
||
| DOID:7400 | Nijmegen breakage syndrome | HGNC:7652 | Homo sapiens (human) | 4683 | NBN |
|
||
| DOID:11725 | Cornelia de Lange syndrome | HGNC:28862 | Homo sapiens (human) | 25836 | NIPBL |
|
||
| DOID:332 | amyotrophic lateral sclerosis | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
|
