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 **6751 - 6775** of **12216** in total

« First

‹ Prev

…

267

268

269

270

271

272

273

274

275

…

Next ›

Last »
Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol ▲	Evidence Code Names	References
DOID:0111240	congenital muscular dystrophy-dystroglycanopathy type A2	SGD:S000005848	Saccharomyces cerevisiae S288C	854499	PMT3	evidence used in automatic assertion	MGI:6194238
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0110297	autosomal recessive limb-girdle muscular dystrophy type 2K	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0111237	congenital muscular dystrophy-dystroglycanopathy type A1	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0050560	Walker-Warburg syndrome	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:27358400
DOID:0112374	muscular dystrophy-dystroglycanopathy	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0050453	lissencephaly	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0050700	cardiomyopathy	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:9884	muscular dystrophy	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:9296	cleft lip	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
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	HGNC:9155	Homo sapiens (human)	5406	PNLIP	evidence used in automatic assertion	MGI:6194238
DOID:10283	prostate cancer	HGNC:9156	Homo sapiens (human)	5407	PNLIPRP1	expression pattern evidence used in manual assertion	PMID:11384102
DOID:653	purine-pyrimidine metabolic disorder	HGNC:7892	Homo sapiens (human)	4860	PNP	inference by association of genotype from phenotype used in manual assertion	PMID:3029074
DOID:5813	purine nucleoside phosphorylase deficiency	HGNC:7892	Homo sapiens (human)	4860	PNP	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 RGD:7240710
DOID:5813	purine nucleoside phosphorylase deficiency	SGD:S000004199	Saccharomyces cerevisiae S288C	850906	PNP1	evidence used in automatic assertion	MGI:6194238
DOID:653	purine-pyrimidine metabolic disorder	SGD:S000004199	Saccharomyces cerevisiae S288C	850906	PNP1	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	HGNC:30802	Homo sapiens (human)	57104	PNPLA2	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