GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Alliance of Genome Resources ID

Species

Gene ID

Gene Symbol

FlyGlycoDB

Evidence Code Names

References

Display
results per page.

Clear

Submissions

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

Displaying entries **1026 - 1050** of **12216** in total

« First

‹ Prev

…

38

39

40

41

42

43

44

45

46

…

Next ›

Last »
Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID ▼	Gene Symbol	Evidence Code Names	References
DOID:0112380	muscular dystrophy-dystroglycanopathy type B2	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
DOID:0110298	autosomal recessive limb-girdle muscular dystrophy type 2N	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
DOID:0050560	Walker-Warburg syndrome	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
DOID:0111240	congenital muscular dystrophy-dystroglycanopathy type A2	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
DOID:0112374	muscular dystrophy-dystroglycanopathy	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
DOID:0014667	disease of metabolism	SGD:S000000036	Saccharomyces cerevisiae S288C	851193	CDC19	evidence used in automatic assertion	MGI:6194238
DOID:4195	hyperglycemia	SGD:S000000036	Saccharomyces cerevisiae S288C	851193	CDC19	evidence used in automatic assertion	MGI:6194238
DOID:10763	hypertension	SGD:S000000036	Saccharomyces cerevisiae S288C	851193	CDC19	evidence used in automatic assertion	MGI:6194238
DOID:0080208	metabolic dysfunction-associated steatotic liver disease	SGD:S000000036	Saccharomyces cerevisiae S288C	851193	CDC19	evidence used in automatic assertion	MGI:6194238
DOID:5204	fructose-1,6-bisphosphatase deficiency	SGD:S000004369	Saccharomyces cerevisiae S288C	851092	FBP1	evidence used in automatic assertion	MGI:6194238
DOID:2978	carbohydrate metabolic disorder	SGD:S000004346	Saccharomyces cerevisiae S288C	851068	TAL1	evidence used in automatic assertion	MGI:6194238
DOID:331	central nervous system disease	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:25351951
DOID:14330	Parkinson's disease	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	evidence used in automatic assertion	MGI:6194238
DOID:1289	neurodegenerative disease	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:25351951
DOID:0111442	optic atrophy 9	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:33028849
DOID:1891	optic nerve disease	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:25351951
DOID:0050883	infantile cerebellar-retinal degeneration	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	evidence used in automatic assertion	MGI:6194238
DOID:1826	epilepsy	SGD:S000004274	Saccharomyces cerevisiae S288C	850990	ECI1	evidence used in automatic assertion	MGI:6194238
DOID:9352	type 2 diabetes mellitus	SGD:S000004263	Saccharomyces cerevisiae S288C	850979	PIG1	evidence used in automatic assertion	MGI:6194238
DOID:1574	alcohol use disorder	SGD:S000004263	Saccharomyces cerevisiae S288C	850979	PIG1	evidence used in automatic assertion	MGI:6194238
DOID:3534	Lafora disease	SGD:S000004248	Saccharomyces cerevisiae S288C	850962	GSY2	evidence used in automatic assertion	MGI:6194238
DOID:1287	cardiovascular system disease	SGD:S000004248	Saccharomyces cerevisiae S288C	850962	GSY2	evidence used in automatic assertion	MGI:6194238
DOID:2747	glycogen storage disease	SGD:S000004248	Saccharomyces cerevisiae S288C	850962	GSY2	evidence used in automatic assertion	MGI:6194238
DOID:5813	purine nucleoside phosphorylase deficiency	SGD:S000004199	Saccharomyces cerevisiae S288C	850906	PNP1	evidence used in automatic assertion	MGI:6194238

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements