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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:850	lung disease	HGNC:10802	Homo sapiens (human)	6440	SFTPC	inference by association of genotype from phenotype used in manual assertion	PMID:11207353 PMID:16910460
DOID:12401	intermittent explosive disorder	HGNC:2228	Homo sapiens (human)	1312	COMT	inference by association of genotype from phenotype used in manual assertion	PMID:11204347
DOID:3068	glioblastoma	HGNC:9884	Homo sapiens (human)	5925	RB1	direct assay evidence used in manual assertion	PMID:11204276
DOID:1612	breast cancer	HGNC:795	Homo sapiens (human)	472	ATM	inference by association of genotype from phenotype used in manual assertion	PMID:11200774 RGD:7240710
DOID:9744	type 1 diabetes mellitus	HGNC:5993	Homo sapiens (human)	3554	IL1R1	inference by association of genotype from phenotype used in manual assertion	PMID:11197691 PMID:8911996
DOID:9970	obesity	HGNC:7842	Homo sapiens (human)	4828	NMB	inference by association of genotype from phenotype used in manual assertion	PMID:11194934 PMID:15585758
DOID:8893	psoriasis	HGNC:43	Homo sapiens (human)	6890	TAP1	inference by association of genotype from phenotype used in manual assertion	PMID:11194890
DOID:7148	rheumatoid arthritis	HGNC:5991	Homo sapiens (human)	3552	IL1A	direct assay evidence used in manual assertion	PMID:11192540
DOID:0060001	withdrawal disorder	RGD:620218	Rattus norvegicus (Norway rat)	81646	Creb1	direct assay evidence used in manual assertion	PMID:11181917 PMID:11331423 PMID:23035088 PMID:25392083 PMID:25711798 PMID:31042569
DOID:6000	congestive heart failure	RGD:3346	Rattus norvegicus (Norway rat)	24655	Plcd1	direct assay evidence used in manual assertion	PMID:11181012
DOID:12120	pulmonary alveolar proteinosis	HGNC:2434	Homo sapiens (human)	1437	CSF2	direct assay evidence used in manual assertion	PMID:11179134 PMID:21478218 PMID:9763547
DOID:3083	chronic obstructive pulmonary disease	HGNC:11892	Homo sapiens (human)	7124	TNF	inference by association of genotype from phenotype used in manual assertion	PMID:11179116 PMID:12537602 PMID:20299531 PMID:20352242
DOID:14453	farmer's lung	HGNC:11892	Homo sapiens (human)	7124	TNF	inference by association of genotype from phenotype used in manual assertion	PMID:11179110
DOID:14453	farmer's lung	HGNC:11892	Homo sapiens (human)	7124	TNF	direct assay evidence used in manual assertion	PMID:11179110
DOID:5844	myocardial infarction	RGD:621316	Rattus norvegicus (Norway rat)	81686	Mmp2	direct assay evidence used in manual assertion	PMID:11179039
DOID:8986	narcolepsy	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:11179016
DOID:8986	narcolepsy	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:11179016
DOID:8986	narcolepsy	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:11179016
DOID:11589	Riley-Day syndrome	HGNC:5959	Homo sapiens (human)	8518	ELP1	inference by association of genotype from phenotype used in manual assertion	PMID:11179008 PMID:11179021 RGD:7240710
DOID:4330	non-Langerhans-cell histiocytosis	HGNC:9360	Homo sapiens (human)	5551	PRF1	inference by association of genotype from phenotype used in manual assertion	PMID:11179007
DOID:0060251	sclerosteosis	HGNC:13771	Homo sapiens (human)	50964	SOST	inference by association of genotype from phenotype used in manual assertion	PMID:11179006
DOID:10584	retinitis pigmentosa	HGNC:10024	Homo sapiens (human)	6017	RLBP1	inference by association of genotype from phenotype used in manual assertion	PMID:11176989
DOID:4154	dentinogenesis imperfecta	HGNC:3054	Homo sapiens (human)	1834	DSPP	inference by association of genotype from phenotype used in manual assertion	PMID:11175790 RGD:7240710
DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome	HGNC:1092	Homo sapiens (human)	668	FOXL2	inference by association of genotype from phenotype used in manual assertion	PMID:11175783 RGD:7240710
DOID:1712	aortic valve stenosis	HGNC:3327	Homo sapiens (human)	2006	ELN	inference by association of genotype from phenotype used in manual assertion	PMID:11175284

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