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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:2986	IgA glomerulonephritis	HGNC:10720	Homo sapiens (human)	6402	SELL	inference by association of genotype from phenotype used in manual assertion	PMID:11828340
DOID:2986	IgA glomerulonephritis	HGNC:10718	Homo sapiens (human)	6401	SELE	inference by association of genotype from phenotype used in manual assertion	PMID:11828340
DOID:0050700	cardiomyopathy	MGI:94885	Mus musculus (house mouse)	13346	Des	author statement supported by traceable reference	PMID:11827695
DOID:10762	portal hypertension	RGD:3329	Rattus norvegicus (Norway rat)	25513	Pik3r1	direct assay evidence used in manual assertion	PMID:11826414
DOID:9074	systemic lupus erythematosus	HGNC:11159	Homo sapiens (human)	6633	SNRPD2	direct assay evidence used in manual assertion	PMID:11823543
DOID:0060170	generalized epilepsy with febrile seizures plus	HGNC:10585	Homo sapiens (human)	6323	SCN1A	inference by association of genotype from phenotype used in manual assertion	PMID:11823106
DOID:707	B-cell lymphoma	HGNC:6006	Homo sapiens (human)	50615	IL21R	inference by association of genotype from phenotype used in manual assertion	PMID:11821949
DOID:0050745	diffuse large B-cell lymphoma	HGNC:6006	Homo sapiens (human)	50615	IL21R	inference by association of genotype from phenotype used in manual assertion	PMID:11821949
DOID:0050424	familial adenomatous polyposis	HGNC:7527	Homo sapiens (human)	4595	MUTYH	inference by association of genotype from phenotype used in manual assertion	PMID:11818965
DOID:0110861	autosomal recessive polycystic kidney disease	MGI:97603	Mus musculus (house mouse)	18763	Pkd1	author statement supported by traceable reference	PMID:11818962 PMID:20053665
DOID:10286	prostate carcinoma	HGNC:6065	Homo sapiens (human)	3623	INHA	inference by association of genotype from phenotype used in manual assertion	PMID:11818495
DOID:1574	alcohol use disorder	RGD:68438	Rattus norvegicus (Norway rat)	29256	Oprl1	mutant phenotype evidence used in manual assertion	PMID:11814626
DOID:3070	high grade glioma	HGNC:11892	Homo sapiens (human)	7124	TNF	mutant phenotype evidence used in manual assertion	PMID:11810046
DOID:14330	Parkinson's disease	HGNC:7872	Homo sapiens (human)	4842	NOS1	inference by association of genotype from phenotype used in manual assertion	PMID:11809160
DOID:7693	abdominal aortic aneurysm	HGNC:9040	Homo sapiens (human)	7941	PLA2G7	inference by association of genotype from phenotype used in manual assertion	PMID:11807372
DOID:3144	cutis laxa	MGI:1346091	Mus musculus (house mouse)	23876	Fbln5	author statement supported by traceable reference	PMID:11805834 PMID:11805835
DOID:0070253	congenital disorder of glycosylation type IIa	MGI:2384966	Mus musculus (house mouse)	217664	Mgat2	author statement supported by traceable reference	PMID:11805078
DOID:5419	schizophrenia	HGNC:2159	Homo sapiens (human)	1268	CNR1	inference by association of genotype from phenotype used in manual assertion	PMID:11803524 PMID:15613777
DOID:8725	vascular dementia	HGNC:9205	Homo sapiens (human)	5445	PON2	inference by association of genotype from phenotype used in manual assertion	PMID:11803456
DOID:10652	Alzheimer's disease	HGNC:9205	Homo sapiens (human)	5445	PON2	inference by association of genotype from phenotype used in manual assertion	PMID:11803456 PMID:16319130
DOID:2841	asthma	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:11802952 PMID:12890388 PMID:19052351 PMID:20159242 PMID:20214848 PMID:20298583
DOID:0090005	Schwartz-Jampel syndrome 1	MGI:96257	Mus musculus (house mouse)	15530	Hspg2	author statement supported by traceable reference	PMID:11802174 PMID:17213231 PMID:18647752 PMID:22449950
DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia	MGI:96257	Mus musculus (house mouse)	15530	Hspg2	author statement supported by traceable reference	PMID:11802174 PMID:12814946
DOID:0110156	Charcot-Marie-Tooth disease type 2B1	MGI:96794	Mus musculus (house mouse)	16905	Lmna	author statement supported by traceable reference	PMID:11799477
DOID:0060490	Schimke immuno-osseous dysplasia	HGNC:11102	Homo sapiens (human)	50485	SMARCAL1	inference by association of genotype from phenotype used in manual assertion	PMID:11799392 RGD:7240710

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