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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

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References ▼
DOID:12894	Sjogren's syndrome	HGNC:6018	Homo sapiens (human)	3569	IL6	inference by association of genotype from phenotype used in manual assertion	PMID:11426023
DOID:5419	schizophrenia	HGNC:6470	Homo sapiens (human)	3897	L1CAM	inference by association of genotype from phenotype used in manual assertion	PMID:11425011
DOID:10652	Alzheimer's disease	HGNC:6701	Homo sapiens (human)	4043	LRPAP1	inference by association of genotype from phenotype used in manual assertion	PMID:11425005
DOID:0060903	thrombosis	RGD:70553	Rattus norvegicus (Norway rat)	113959	C5ar1	mutant phenotype evidence used in manual assertion	PMID:11422211
DOID:0060692	platelet-type bleeding disorder 8	MGI:1918089	Mus musculus (house mouse)	70839	P2ry12	author statement supported by traceable reference	PMID:11413167 PMID:12897207
DOID:684	hepatocellular carcinoma	HGNC:2433	Homo sapiens (human)	1436	CSF1R	direct assay evidence used in manual assertion	PMID:11412385 PMID:32724427
DOID:13241	Behcet's disease	HGNC:5344	Homo sapiens (human)	3383	ICAM1	inference by association of genotype from phenotype used in manual assertion	PMID:11409120 PMID:12808331
DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type	MGI:96702	Mus musculus (house mouse)	110308	Krt5	author statement supported by traceable reference	PMID:11408584
DOID:13042	persistent fetal circulation syndrome	HGNC:2323	Homo sapiens (human)	1373	CPS1	inference by association of genotype from phenotype used in manual assertion	PMID:11407344
DOID:0050771	pheochromocytoma	HGNC:10681	Homo sapiens (human)	6390	SDHB	inference by association of genotype from phenotype used in manual assertion	PMID:11404820
DOID:0050773	paraganglioma	HGNC:10681	Homo sapiens (human)	6390	SDHB	inference by association of genotype from phenotype used in manual assertion	PMID:11404820 RGD:7240710
DOID:2938	Epstein-Barr virus infectious disease	HGNC:4940	Homo sapiens (human)	3115	HLA-DPB1	inference by association of genotype from phenotype used in manual assertion	PMID:11401923
DOID:8947	diabetic retinopathy	HGNC:6709	Homo sapiens (human)	4049	LTA	inference by association of genotype from phenotype used in manual assertion	PMID:11399938
DOID:2841	asthma	HGNC:6015	Homo sapiens (human)	3566	IL4R	direct assay evidence used in manual assertion	PMID:11398072 PMID:16917945
DOID:10825	essential hypertension	HGNC:7876	Homo sapiens (human)	4846	NOS3	inference by association of genotype from phenotype used in manual assertion	PMID:11394896 PMID:9084930
DOID:5844	myocardial infarction	HGNC:333	Homo sapiens (human)	183	AGT	inference by association of genotype from phenotype used in manual assertion	PMID:11393670 PMID:17299437
DOID:0081267	graft-versus-host disease	HGNC:4893	Homo sapiens (human)	3082	HGF	direct assay evidence used in manual assertion	PMID:11390418
DOID:0110154	Charcot-Marie-Tooth disease type 2A1	HGNC:16636	Homo sapiens (human)	23095	KIF1B	inference by association of genotype from phenotype used in manual assertion	PMID:11389829 RGD:7240710
DOID:2734	keratosis follicularis	MGI:88110	Mus musculus (house mouse)	11938	Atp2a2	author statement supported by traceable reference	PMID:11389134
DOID:3908	lung non-small cell carcinoma	HGNC:1753	Homo sapiens (human)	1012	CDH13	direct assay evidence used in manual assertion	PMID:11389090
DOID:3459	breast carcinoma	HGNC:1753	Homo sapiens (human)	1012	CDH13	direct assay evidence used in manual assertion	PMID:11389090
DOID:409	liver disease	HGNC:11892	Homo sapiens (human)	7124	TNF	inference by association of genotype from phenotype used in manual assertion	PMID:11389006
DOID:2352	hemochromatosis	HGNC:11892	Homo sapiens (human)	7124	TNF	inference by association of genotype from phenotype used in manual assertion	PMID:11389006 PMID:16793930
DOID:9352	type 2 diabetes mellitus	MGI:104874	Mus musculus (house mouse)	11652	Akt2	author statement supported by traceable reference	PMID:11387480
DOID:8778	Crohn's disease	HGNC:5331	Homo sapiens (human)	64127	NOD2	inference by association of genotype from phenotype used in manual assertion	PMID:11385576 PMID:21983784 RGD:7240710

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