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:0111305 | familial febrile seizures 4 | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
|
||
| DOID:1827 | idiopathic generalized epilepsy | HGNC:16882 | Homo sapiens (human) | 10021 | HCN4 |
|
||
| DOID:1485 | cystic fibrosis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
|
||
| DOID:0060009 | MHC class I deficiency | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
|
||
| DOID:0080494 | ovarian dysgenesis 2 | HGNC:1068 | Homo sapiens (human) | 9210 | BMP15 |
|
||
| DOID:14671 | multiple intestinal atresia | HGNC:19750 | Homo sapiens (human) | 57217 | TTC7A |
|
||
| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:6482 | Homo sapiens (human) | 3908 | LAMA2 |
|
||
| DOID:0111421 | familial apolipoprotein A5 deficiency | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
|
||
| DOID:0081401 | autosomal dominant distal hereditary motor neuronopathy 13 | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
|
||
| DOID:0070150 | hereditary sensory and autonomic neuropathy type 2B | HGNC:25964 | Homo sapiens (human) | 54463 | RETREG1 |
|
||
| DOID:0110664 | congenital myasthenic syndrome 3C | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
|
||
| DOID:0080960 | amelogenesis imperfecta type 2A6 | HGNC:4519 | Homo sapiens (human) | 8111 | GPR68 |
|
||
| DOID:0112106 | chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
|
||
| DOID:0111268 | autosomal recessive hyaline body myopathy | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
|
||
| DOID:0050576 | Senior-Loken syndrome | HGNC:17861 | Homo sapiens (human) | 26146 | TRAF3IP1 |
|
||
| DOID:9119 | acute myeloid leukemia | HGNC:16063 | Homo sapiens (human) | 8028 | MLLT10 |
|
||
| DOID:0111634 | autosomal recessive nonsyndromic deafness 99 | HGNC:26991 | Homo sapiens (human) | 124842 | TMEM132E |
|
||
| DOID:0060772 | multiple types of congenital heart defects 6 | HGNC:4214 | Homo sapiens (human) | 2657 | GDF1 |
|
||
| DOID:0112228 | lissencephaly 9 with complex brainstem malformation | HGNC:13664 | Homo sapiens (human) | 23499 | MACF1 |
|
||
| DOID:0110654 | long QT syndrome 13 | HGNC:6266 | Homo sapiens (human) | 3762 | KCNJ5 |
|
||
| DOID:0111467 | combined oxidative phosphorylation deficiency 13 | HGNC:23166 | Homo sapiens (human) | 87178 | PNPT1 |
|
||
| DOID:0080512 | Meier-Gorlin syndrome 1 | HGNC:8487 | Homo sapiens (human) | 4998 | ORC1 |
|
||
| DOID:0080735 | Ehlers-Danlos syndrome kyphoscoliotic type 2 | HGNC:18625 | Homo sapiens (human) | 55033 | FKBP14 |
|
||
| DOID:0050650 | familial atrial fibrillation | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
|
||
| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
|
