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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	October 9, 2024

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID ▲	Gene Symbol	Evidence Code Names	References
DOID:8805	intermediate coronary syndrome	SGD:S000004442	Saccharomyces cerevisiae S288C	851171	HMG2	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:0014667	disease of metabolism	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:0111240	congenital muscular dystrophy-dystroglycanopathy type A2	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:0050560	Walker-Warburg syndrome	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:0112374	muscular dystrophy-dystroglycanopathy	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:9884	muscular dystrophy	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:9970	obesity	SGD:S000000054	Saccharomyces cerevisiae S288C	851241	CNE1	evidence used in automatic assertion	MGI:6194238
DOID:0060269	pontocerebellar hypoplasia type 2C	SGD:S000000066	Saccharomyces cerevisiae S288C	851267	SEN34	evidence used in automatic assertion	MGI:6194238
DOID:3969	thyroid gland papillary carcinoma	SGD:S000000094	Saccharomyces cerevisiae S288C	851299	PHO11	evidence used in automatic assertion	MGI:6194238
DOID:0112333	pontocerebellar hypoplasia type 16	SGD:S000000094	Saccharomyces cerevisiae S288C	851299	PHO11	evidence used in automatic assertion	MGI:6194238
DOID:0060559	lethal congenital contracture syndrome 1	SGD:S000002366	Saccharomyces cerevisiae S288C	851320	GLE1	evidence used in automatic assertion genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:24243016
DOID:0070539	Halperin-Birk syndrome	SGD:S000002354	Saccharomyces cerevisiae S288C	851332	SEC31	evidence used in automatic assertion	MGI:6194238
DOID:83	cataract	SGD:S000002405	Saccharomyces cerevisiae S288C	851351	SOR2	evidence used in automatic assertion	MGI:6194238
DOID:0081427	autosomal recessive distal hereditary motor neuronopathy 8	SGD:S000002405	Saccharomyces cerevisiae S288C	851351	SOR2	evidence used in automatic assertion	MGI:6194238
DOID:9743	diabetic neuropathy	SGD:S000002405	Saccharomyces cerevisiae S288C	851351	SOR2	evidence used in automatic assertion	MGI:6194238
DOID:0060410	chromosome 1p36 deletion syndrome	HGNC:6229	Homo sapiens (human)	8514	KCNAB2	evidence used in automatic assertion	MGI:6194238
DOID:0050548	hereditary sensory neuropathy	SGD:S000002302	Saccharomyces cerevisiae S288C	851412	CCT4	evidence used in automatic assertion	MGI:6194238

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