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:10762 | portal hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
DOID:3492 | mixed connective tissue disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
DOID:12662 | paracoccidioidomycosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
DOID:0080162 | lupus nephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
DOID:3083 | chronic obstructive pulmonary disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
DOID:841 | extrinsic allergic alveolitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
|
||
DOID:1826 | epilepsy | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
|
||
DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
|
||
DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
|
||
DOID:10534 | stomach cancer | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
|
||
DOID:0060060 | non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
|
||
DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
|
||
DOID:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
|
||
DOID:0050571 | congenital disorder of glycosylation type II | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
|
||
DOID:2841 | asthma | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
|
||
DOID:8677 | perinatal necrotizing enterocolitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
|
||
DOID:4483 | rhinitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
|
||
DOID:399 | tuberculosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
|
||
DOID:13564 | aspergillosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
|
||
DOID:0060000 | infective endocarditis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
|
||
DOID:874 | bacterial pneumonia | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
|
||
DOID:3021 | acute kidney failure | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
|
||
DOID:4989 | pancreatitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
|
||
DOID:2841 | asthma | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
|
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 v4.0.0
Last updated: August 19, 2024