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:12858 | Huntington's disease | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
|
||
DOID:3908 | lung non-small cell carcinoma | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
|
||
DOID:9352 | type 2 diabetes mellitus | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
|
||
DOID:219 | colon cancer | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
|
||
DOID:9970 | obesity | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
|
||
DOID:13580 | cholestasis | MGI:2145955 | Mus musculus (house mouse) | 105787 | Prkaa1 |
|
||
DOID:0070114 | Niemann-Pick disease type C2 | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
|
||
DOID:14504 | Niemann-Pick disease | HGNC:14537 | Homo sapiens (human) | 10577 | NPC2 |
|
||
DOID:1508 | candidiasis | HGNC:1615 | Homo sapiens (human) | 10576 | CCT2 |
|
||
DOID:14791 | Leber congenital amaurosis | HGNC:1615 | Homo sapiens (human) | 10576 | CCT2 |
|
||
DOID:0060036 | intrinsic cardiomyopathy | HGNC:1617 | Homo sapiens (human) | 10575 | CCT4 |
|
||
DOID:0050548 | hereditary sensory neuropathy | HGNC:1617 | Homo sapiens (human) | 10575 | CCT4 |
|
||
DOID:0110055 | amelogenesis imperfecta type 3A | MGI:2145900 | Mus musculus (house mouse) | 105732 | Fam83h |
|
||
DOID:11832 | visual epilepsy | MGI:2145895 | Mus musculus (house mouse) | 105727 | Slc38a1 |
|
||
DOID:684 | hepatocellular carcinoma | MGI:2145895 | Mus musculus (house mouse) | 105727 | Slc38a1 |
|
||
DOID:0111052 | Scott syndrome | MGI:2145890 | Mus musculus (house mouse) | 105722 | Ano6 |
|
||
DOID:0050589 | inflammatory bowel disease | MGI:2145890 | Mus musculus (house mouse) | 105722 | Ano6 |
|
||
DOID:7147 | ankylosing spondylitis | MGI:2145890 | Mus musculus (house mouse) | 105722 | Ano6 |
|
||
DOID:936 | brain disease | MGI:2179432 | Mus musculus (house mouse) | 105689 | Mycbp2 |
|
||
DOID:12117 | pulmonary alveolar microlithiasis | HGNC:11020 | Homo sapiens (human) | 10568 | SLC34A2 |
|
||
DOID:0050454 | periventricular nodular heterotopia | HGNC:15853 | Homo sapiens (human) | 10564 | ARFGEF2 |
|
||
DOID:0090117 | thiamine-responsive megaloblastic anemia syndrome | HGNC:10938 | Homo sapiens (human) | 10560 | SLC19A2 |
|
||
DOID:13382 | megaloblastic anemia | HGNC:10938 | Homo sapiens (human) | 10560 | SLC19A2 |
|
||
DOID:9351 | diabetes mellitus | HGNC:10938 | Homo sapiens (human) | 10560 | SLC19A2 |
|
||
DOID:784 | chronic kidney disease | HGNC:10938 | Homo sapiens (human) | 10560 | SLC19A2 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024