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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 **276 - 300** 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:676	juvenile rheumatoid arthritis	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:10457895
DOID:583	hemolytic anemia	HGNC:10006	Homo sapiens (human)	6005	RHAG	inference by association of genotype from phenotype used in manual assertion	PMID:10467273
DOID:12134	factor VIII deficiency	HGNC:3546	Homo sapiens (human)	2157	F8	mutant phenotype evidence used in manual assertion	PMID:10468616
DOID:12361	Graves' disease	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:10468909 PMID:11272094
DOID:3512	neurofibrosarcoma	HGNC:7534	Homo sapiens (human)	4601	MXI1	inference by association of genotype from phenotype used in manual assertion	PMID:10470286
DOID:14067	Plasmodium falciparum malaria	HGNC:2621	Homo sapiens (human)	1557	CYP2C19	inference by association of genotype from phenotype used in manual assertion	PMID:10471063
DOID:2893	cervix carcinoma	HGNC:3690	Homo sapiens (human)	2261	FGFR3	inference by association of genotype from phenotype used in manual assertion	PMID:10471491 PMID:11114733
DOID:11054	urinary bladder cancer	HGNC:3690	Homo sapiens (human)	2261	FGFR3	inference by association of genotype from phenotype used in manual assertion	PMID:10471491 PMID:18166262 PMID:18231634 RGD:7240710
DOID:381	arthropathy	HGNC:12771	Homo sapiens (human)	8838	CCN6	inference by association of genotype from phenotype used in manual assertion	PMID:10471507
DOID:446	primary hyperaldosteronism	MGI:95824	Mus musculus (house mouse)	14815	Nr3c1	author statement supported by traceable reference	PMID:10471508
DOID:12336	male infertility	MGI:88547	Mus musculus (house mouse)	13000	Csnk2a2	author statement supported by traceable reference	PMID:10471512
DOID:13359	Ehlers-Danlos syndrome	HGNC:930	Homo sapiens (human)	11285	B4GALT7	inference by association of genotype from phenotype used in manual assertion	PMID:10473568
DOID:5603	T-cell acute lymphoblastic leukemia	HGNC:8068	Homo sapiens (human)	4928	NUP98	inference by association of genotype from phenotype used in manual assertion	PMID:10477737
DOID:5419	schizophrenia	MGI:95819	Mus musculus (house mouse)	14810	Grin1	author statement supported by traceable reference	PMID:10481908
DOID:0110436	dilated cardiomyopathy 1L	MGI:1346525	Mus musculus (house mouse)	24052	Sgcd	author statement supported by traceable reference	PMID:10481911 PMID:10862711 PMID:23695275
DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F	MGI:1346525	Mus musculus (house mouse)	24052	Sgcd	author statement supported by traceable reference	PMID:10481911 PMID:10862711 PMID:28797108
DOID:14687	diastrophic dysplasia	HGNC:10994	Homo sapiens (human)	1836	SLC26A2	inference by association of genotype from phenotype used in manual assertion	PMID:10482955 RGD:7240710
DOID:2977	primary hyperoxaluria	HGNC:4570	Homo sapiens (human)	9380	GRHPR	inference by association of genotype from phenotype used in manual assertion	PMID:10484776
DOID:3312	bipolar disorder	HGNC:11050	Homo sapiens (human)	6532	SLC6A4	inference by association of genotype from phenotype used in manual assertion	PMID:10484962
DOID:2394	ovarian cancer	HGNC:7155	Homo sapiens (human)	4312	MMP1	inference by association of genotype from phenotype used in manual assertion	PMID:10485461
DOID:9074	systemic lupus erythematosus	MGI:104879	Mus musculus (house mouse)	18566	Pdcd1	author statement supported by traceable reference	PMID:10485649 PMID:9796923
DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C	MGI:1346524	Mus musculus (house mouse)	24053	Sgcg	author statement supported by traceable reference	PMID:10485893 PMID:12609501 PMID:14982859 PMID:9732288
DOID:0050711	aceruloplasminemia	MGI:88476	Mus musculus (house mouse)	12870	Cp	author statement supported by traceable reference	PMID:10485908 PMID:11461924 PMID:18804145
DOID:5844	myocardial infarction	HGNC:6169	Homo sapiens (human)	3700	ITIH4	direct assay evidence used in manual assertion	PMID:10486281
DOID:8805	intermediate coronary syndrome	HGNC:6169	Homo sapiens (human)	3700	ITIH4	direct assay evidence used in manual assertion	PMID:10486281

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