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:6000 | congestive heart failure | HGNC:1953 | Homo sapiens (human) | 1132 | CHRM4 |
|
||
DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
|
||
DOID:6432 | pulmonary hypertension | HGNC:13708 | Homo sapiens (human) | 11318 | GPR182 |
|
||
DOID:0060370 | Parkinson's disease 7 | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
|
||
DOID:8466 | retinal degeneration | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
|
||
DOID:3526 | cerebral infarction | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
|
||
DOID:14330 | Parkinson's disease | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
|
||
DOID:0080855 | Parkinsonism | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
|
||
DOID:0060894 | early-onset Parkinson's disease | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
|
||
DOID:3525 | middle cerebral artery infarction | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
|
||
DOID:2841 | asthma | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
|
||
DOID:3083 | chronic obstructive pulmonary disease | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
|
||
DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
|
||
DOID:365 | bladder disease | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
|
||
DOID:0060889 | prune belly syndrome | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
|
||
DOID:0050685 | small cell carcinoma | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
|
||
DOID:3770 | pulmonary fibrosis | HGNC:1952 | Homo sapiens (human) | 1131 | CHRM3 |
|
||
DOID:3571 | liver cancer | HGNC:10962 | Homo sapiens (human) | 11309 | SLCO2B1 |
|
||
DOID:1793 | pancreatic cancer | HGNC:10962 | Homo sapiens (human) | 11309 | SLCO2B1 |
|
||
DOID:0050817 | Stargardt disease | MGI:109424 | Mus musculus (house mouse) | 11304 | Abca4 |
|
||
DOID:0110354 | retinitis pigmentosa 19 | MGI:109424 | Mus musculus (house mouse) | 11304 | Abca4 |
|
||
DOID:0111013 | cone-rod dystrophy 3 | MGI:109424 | Mus musculus (house mouse) | 11304 | Abca4 |
|
||
DOID:10584 | retinitis pigmentosa | MGI:109424 | Mus musculus (house mouse) | 11304 | Abca4 |
|
||
DOID:8466 | retinal degeneration | MGI:109424 | Mus musculus (house mouse) | 11304 | Abca4 |
|
||
DOID:8501 | fundus dystrophy | MGI:109424 | Mus musculus (house mouse) | 11304 | Abca4 |
|
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