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:0060743 | methylmalonic acidemia cblB type | HGNC:19331 | Homo sapiens (human) | 326625 | MMAB |
|
||
| DOID:0111390 | mucopolysaccharidosis Ih | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
|
||
| DOID:9258 | Waardenburg syndrome | HGNC:6343 | Homo sapiens (human) | 4254 | KITLG |
|
||
| DOID:12365 | malaria | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
|
||
| DOID:1612 | breast cancer | HGNC:5012 | Homo sapiens (human) | 3161 | HMMR |
|
||
| DOID:0110985 | Joubert syndrome 16 | HGNC:26944 | Homo sapiens (human) | 51524 | TMEM138 |
|
||
| DOID:612 | primary immunodeficiency disease | HGNC:17967 | Homo sapiens (human) | 51135 | IRAK4 |
|
||
| DOID:0111376 | fetal akinesia deformation sequence syndrome 3 | HGNC:26594 | Homo sapiens (human) | 285489 | DOK7 |
|
||
| DOID:0111686 | hereditary mixed polyposis syndrome 2 | HGNC:1076 | Homo sapiens (human) | 657 | BMPR1A |
|
||
| DOID:0111380 | solitary median maxillary central incisor | HGNC:10848 | Homo sapiens (human) | 6469 | SHH |
|
||
| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
|
||
| DOID:0110247 | cataract 36 | HGNC:30831 | Homo sapiens (human) | 23424 | TDRD7 |
|
||
| DOID:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
|
||
| DOID:0111984 | immunodeficiency 58 | HGNC:27089 | Homo sapiens (human) | 146206 | CARMIL2 |
|
||
| DOID:0070140 | autosomal recessive cutis laxa type IIC | HGNC:857 | Homo sapiens (human) | 529 | ATP6V1E1 |
|
||
| DOID:0111462 | cardiofaciocutaneous syndrome 3 | HGNC:6840 | Homo sapiens (human) | 5604 | MAP2K1 |
|
||
| DOID:0111438 | optic atrophy 5 | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
|
||
| DOID:0111021 | cone-rod dystrophy 15 | HGNC:14550 | Homo sapiens (human) | 92211 | CDHR1 |
|
||
| DOID:0111232 | congenital muscular dystrophy-dystroglycanopathy type A9 | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
|
||
| DOID:0050998 | nonprogressive cerebellar ataxia with mental retardation | HGNC:18806 | Homo sapiens (human) | 23261 | CAMTA1 |
|
||
| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | HGNC:13941 | Homo sapiens (human) | 80736 | SLC44A4 |
|
||
| DOID:0111923 | spermatogenic failure 42 | HGNC:29936 | Homo sapiens (human) | 83894 | TTC29 |
|
||
| DOID:0060355 | amyotrophic lateral sclerosis type 22 | HGNC:12407 | Homo sapiens (human) | 7277 | TUBA4A |
|
||
| DOID:0112231 | lissencephaly 7 with cerebellar hypoplasia | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
|
||
| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
|
