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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▲ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2384 | Wernicke encephalopathy | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
|
||
| DOID:0050773 | paraganglioma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
|
||
| DOID:0110644 | long QT syndrome 1 | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
|
||
| DOID:2957 | pulmonary tuberculosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
|
||
| DOID:0111141 | delayed sleep phase syndrome | HGNC:2384 | Homo sapiens (human) | 1407 | CRY1 |
|
||
| DOID:0050866 | oral squamous cell carcinoma | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
|
||
| DOID:1907 | malignant fibrous histiocytoma | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:3070 | high grade glioma | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
|
||
| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
|
||
| DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
|
||
| DOID:162 | cancer | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
|
||
| DOID:10325 | silicosis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
|
||
| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
|
||
| DOID:7998 | hyperthyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
|
||
| DOID:1793 | pancreatic cancer | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
|
||
| DOID:3827 | congenital diaphragmatic hernia | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
|
||
| DOID:2476 | hereditary spastic paraplegia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
|
||
| DOID:2352 | hemochromatosis | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
|
||
| DOID:10140 | dry eye syndrome | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
|
||
| DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
|
||
| DOID:9452 | steatotic liver disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
|
||
| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
|
||
| DOID:0014667 | disease of metabolism | HGNC:8877 | Homo sapiens (human) | 5213 | PFKM |
|
