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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

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Disease ID	Disease Name	Alliance of Genome Resources ID ▼	Species	Gene ID	Gene Symbol	Evidence Code Names	References
DOID:1588	thrombocytopenia	SGD:S000000223	Saccharomyces cerevisiae S288C	852307	GAL10	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:30247636
DOID:9870	galactosemia	SGD:S000000222	Saccharomyces cerevisiae S288C	852306	GAL7	evidence used in automatic assertion genetic interaction evidence used in manual assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:10799308 PMID:24077966 PMID:28213126 PMID:8794735
DOID:0111459	classic galactosemia	SGD:S000000222	Saccharomyces cerevisiae S288C	852306	GAL7	evidence used in automatic assertion	MGI:6194238
DOID:0070433	hyperphosphatasia with impaired intellectual development syndrome 1	SGD:S000000208	Saccharomyces cerevisiae S288C	852289	GPI18	evidence used in automatic assertion	MGI:6194238
DOID:0080556	congenital disorder of glycosylation Id	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:23038983
DOID:5212	congenital disorder of glycosylation	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:10581255
DOID:0080566	congenital disorder of glycosylation In	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:18313027
DOID:162	cancer	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:26354769
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:9884	muscular dystrophy	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
DOID:0050453	lissencephaly	SGD:S000000021	Saccharomyces cerevisiae S288C	851210	PMT2	evidence used in automatic assertion	MGI:6194238
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:0080411	familial adenomatous polyposis 3	SGD:S000000013	Saccharomyces cerevisiae S288C	851218	NTG1	evidence used in automatic assertion	MGI:6194238
DOID:2752	glycogen storage disease II	RGD:735227	Rattus norvegicus (Norway rat)	367562	Gaa	evidence used in automatic assertion	MGI:6194238
DOID:0080562	congenital disorder of glycosylation Ij	RGD:735124	Rattus norvegicus (Norway rat)	300668	Dpagt1	evidence used in automatic assertion	MGI:6194238
DOID:0110676	congenital myasthenic syndrome 13	RGD:735124	Rattus norvegicus (Norway rat)	300668	Dpagt1	evidence used in automatic assertion	MGI:6194238

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