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 **826 - 850** of **12216** in total

« First

‹ Prev

…

30

31

32

33

34

35

36

37

38

…

Next ›

Last »
Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID ▼	Gene Symbol	Evidence Code Names	References
DOID:9884	muscular dystrophy	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:0050453	lissencephaly	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:0111240	congenital muscular dystrophy-dystroglycanopathy type A2	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:0110298	autosomal recessive limb-girdle muscular dystrophy type 2N	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:0112380	muscular dystrophy-dystroglycanopathy type B2	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:0050560	Walker-Warburg syndrome	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:0112374	muscular dystrophy-dystroglycanopathy	SGD:S000003431	Saccharomyces cerevisiae S288C	853113	PMT6	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:0050827	rheumatic heart disease	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:10652	Alzheimer's disease	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:8947	diabetic retinopathy	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:1826	epilepsy	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:0060108	brain glioma	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:3525	middle cerebral artery infarction	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:3319	lymphangioleiomyomatosis	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:0050866	oral squamous cell carcinoma	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238
DOID:2978	carbohydrate metabolic disorder	SGD:S000003275	Saccharomyces cerevisiae S288C	852934	NQM1	evidence used in automatic assertion	MGI:6194238
DOID:10763	hypertension	HGNC:2645	Homo sapiens (human)	8529	CYP4F2	evidence used in automatic assertion	MGI:6194238
DOID:0080572	congenital disorder of glycosylation Iw	SGD:S000002990	Saccharomyces cerevisiae S288C	852862	STT3	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:34653363
DOID:0080573	congenital disorder of glycosylation Ix	SGD:S000002990	Saccharomyces cerevisiae S288C	852862	STT3	evidence used in automatic assertion	MGI:6194238
DOID:0070254	congenital disorder of glycosylation type IIb	SGD:S000002995	Saccharomyces cerevisiae S288C	852857	CWH41	evidence used in automatic assertion	MGI:6194238
DOID:0080470	developmental and epileptic encephalopathy 36	SGD:S000003015	Saccharomyces cerevisiae S288C	852835	ALG13	evidence used in automatic assertion	MGI:6194238
DOID:3651	pyruvate carboxylase deficiency disease	SGD:S000003030	Saccharomyces cerevisiae S288C	852818	PYC1	evidence used in automatic assertion	MGI:6194238
DOID:0080561	congenital disorder of glycosylation Ii	SGD:S000003033	Saccharomyces cerevisiae S288C	852815	ALG2	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