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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 **13901 - 13925** 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:9074	systemic lupus erythematosus	HGNC:2595	Homo sapiens (human)	1543	CYP1A1	inference by association of genotype from phenotype used in manual assertion	PMID:10599336 PMID:14611903 PMID:19561157
DOID:9256	colorectal cancer	HGNC:7127	Homo sapiens (human)	4292	MLH1	inference by association of genotype from phenotype used in manual assertion	PMID:10598809
DOID:552	pneumonia	RGD:3644	Rattus norvegicus (Norway rat)	29397	Ccl11	mutant phenotype evidence used in manual assertion	PMID:10595930
DOID:0050855	renal fibrosis	RGD:2866	Rattus norvegicus (Norway rat)	25712	Ifng	direct assay evidence used in manual assertion	PMID:10594787
DOID:3389	Papillon-Lefevre disease	HGNC:2528	Homo sapiens (human)	1075	CTSC	inference by association of genotype from phenotype used in manual assertion	PMID:10593994 RGD:7240710
DOID:437	myasthenia gravis	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:10593018 PMID:19561379
DOID:437	myasthenia gravis	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:10593018 PMID:19561379
DOID:3393	coronary artery disease	HGNC:6125	Homo sapiens (human)	3667	IRS1	inference by association of genotype from phenotype used in manual assertion	PMID:10591678
DOID:2394	ovarian cancer	HGNC:9393	Homo sapiens (human)	5578	PRKCA	mutant phenotype evidence used in manual assertion	PMID:10589745
DOID:0050477	Liddle syndrome	MGI:104696	Mus musculus (house mouse)	20277	Scnn1b	author statement supported by traceable reference	PMID:10589691
DOID:3687	MELAS syndrome	HGNC:7461	Homo sapiens (human)	4540	MT-ND5	inference by association of genotype from phenotype used in manual assertion	PMID:10589546 PMID:18587274 PMID:21850008
DOID:3687	MELAS syndrome	HGNC:7461	Homo sapiens (human)	4540	ND5	inference by association of genotype from phenotype used in manual assertion	PMID:10589546 PMID:18587274 PMID:21850008
DOID:12801	mucopolysaccharidosis III	MGI:1351641	Mus musculus (house mouse)	27419	Naglu	author statement supported by traceable reference	PMID:10588735 PMID:12576554 PMID:17712420
DOID:5212	congenital disorder of glycosylation	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	sequence similarity evidence used in manual assertion	PMID:10581255
DOID:5212	congenital disorder of glycosylation	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	genetic interaction evidence used in manual assertion	PMID:10581255
DOID:3659	sialuria	HGNC:10933	Homo sapiens (human)	26503	SLC17A5	inference by association of genotype from phenotype used in manual assertion	PMID:10581036 RGD:7240710
DOID:0050590	severe congenital neutropenia	HGNC:3309	Homo sapiens (human)	1991	ELANE	inference by association of genotype from phenotype used in manual assertion	PMID:10581030 PMID:21425445 PMID:24616599
DOID:10584	retinitis pigmentosa	HGNC:9990	Homo sapiens (human)	5995	RGR	inference by association of genotype from phenotype used in manual assertion	PMID:10581022
DOID:9744	type 1 diabetes mellitus	HGNC:1848	Homo sapiens (human)	1056	CEL	direct assay evidence used in manual assertion	PMID:10580419
DOID:11726	Emery-Dreifuss muscular dystrophy	MGI:96794	Mus musculus (house mouse)	16905	Lmna	author statement supported by traceable reference	PMID:10579712 PMID:15548545
DOID:0060193	amyotrophic lateral sclerosis type 1	MGI:98351	Mus musculus (house mouse)	20655	Sod1	author statement supported by traceable reference	PMID:10578106 PMID:15263088 PMID:25468678 PMID:7846037
DOID:10763	hypertension	HGNC:9603	Homo sapiens (human)	5740	PTGIS	inference by association of genotype from phenotype used in manual assertion	PMID:10577996 PMID:12372404 PMID:17070428
DOID:0080301	atypical hemolytic-uremic syndrome	HGNC:4883	Homo sapiens (human)	3075	CFH	inference by association of genotype from phenotype used in manual assertion	PMID:10577907 PMID:17517971 PMID:20513133 RGD:7240710
DOID:0060770	dextro-looped transposition of the great arteries	MGI:109448	Mus musculus (house mouse)	12627	Cfc1	author statement supported by traceable reference	PMID:10574770
DOID:6406	double outlet right ventricle	MGI:109448	Mus musculus (house mouse)	12627	Cfc1	author statement supported by traceable reference	PMID:10574770

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