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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	January 28, 2025

Displaying entries **6001 - 6025** of **14279** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence ▼	References
DOID:5419	schizophrenia	HGNC:6144	Homo sapiens (human)	8516	ITGA8	inference by association of genotype from phenotype used in manual assertion	PMID:23153507
DOID:2030	anxiety disorder	HGNC:4092	Homo sapiens (human)	2571	GAD1	inference by association of genotype from phenotype used in manual assertion	PMID:22328461
DOID:9975	cocaine dependence	HGNC:29944	Homo sapiens (human)	55714	TENM3	inference by association of genotype from phenotype used in manual assertion	PMID:18438686
DOID:0060307	autosomal dominant intellectual developmental disorder	HGNC:10760	Homo sapiens (human)	6418	SET	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080346	blepharocheilodontic syndrome 2	HGNC:2515	Homo sapiens (human)	1500	CTNND1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:684	hepatocellular carcinoma	HGNC:40	Homo sapiens (human)	5243	ABCB1	inference by association of genotype from phenotype used in manual assertion	PMID:23488625 PMID:24175826
DOID:11984	hypertrophic cardiomyopathy	HGNC:333	Homo sapiens (human)	183	AGT	inference by association of genotype from phenotype used in manual assertion	PMID:9023164
DOID:0060564	spinal disease	HGNC:3755	Homo sapiens (human)	2317	FLNB	inference by association of genotype from phenotype used in manual assertion	PMID:14991055
DOID:8029	sporadic breast cancer	HGNC:8912	Homo sapiens (human)	5245	PHB1	inference by association of genotype from phenotype used in manual assertion	PMID:1540973
DOID:0050650	familial atrial fibrillation	HGNC:6294	Homo sapiens (human)	3784	KCNQ1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:10652	Alzheimer's disease	HGNC:8032	Homo sapiens (human)	4915	NTRK2	inference by association of genotype from phenotype used in manual assertion	PMID:18780967
DOID:1793	pancreatic cancer	HGNC:1884	Homo sapiens (human)	1080	CFTR	inference by association of genotype from phenotype used in manual assertion	PMID:16227367
DOID:12347	osteogenesis imperfecta	HGNC:23697	Homo sapiens (human)	23187	PHLDB1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0112224	chondrodysplasia with joint dislocations gPAPP type	HGNC:26019	Homo sapiens (human)	54928	BPNT2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:1324	lung cancer	HGNC:1959	Homo sapiens (human)	1138	CHRNA5	inference by association of genotype from phenotype used in manual assertion	PMID:20587604 PMID:21448929 PMID:29193083 PMID:29993116 PMID:33419953 RGD:7240710
DOID:11394	adult respiratory distress syndrome	HGNC:6922	Homo sapiens (human)	4153	MBL2	inference by association of genotype from phenotype used in manual assertion	PMID:17133182
DOID:6713	cerebrovascular disease	HGNC:333	Homo sapiens (human)	183	AGT	inference by association of genotype from phenotype used in manual assertion	PMID:17220293
DOID:0080594	hyper IgE recurrent infection syndrome 2	HGNC:19191	Homo sapiens (human)	81704	DOCK8	inference by association of genotype from phenotype used in manual assertion	PMID:21763205 RGD:7240710
DOID:12185	otosclerosis	HGNC:333	Homo sapiens (human)	183	AGT	inference by association of genotype from phenotype used in manual assertion	PMID:18491423
DOID:13258	typhoid fever	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:11120931
DOID:0050983	spinocerebellar ataxia type 36	HGNC:15911	Homo sapiens (human)	10528	NOP56	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111144	preterm premature rupture of the membranes	HGNC:1546	Homo sapiens (human)	871	SERPINH1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:784	chronic kidney disease	HGNC:2300	Homo sapiens (human)	1361	CPB2	inference by association of genotype from phenotype used in manual assertion	PMID:19056482
DOID:2841	asthma	HGNC:18274	Homo sapiens (human)	57105	CYSLTR2	inference by association of genotype from phenotype used in manual assertion	PMID:15454733 PMID:15475736
DOID:10487	Hirschsprung's disease	HGNC:4232	Homo sapiens (human)	2668	GDNF	inference by association of genotype from phenotype used in manual assertion	RGD:7240710

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