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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:1474	aggressive periodontitis	HGNC:6018	Homo sapiens (human)	3569	IL6	inference by association of genotype from phenotype used in manual assertion	PMID:28662328
DOID:0060409	NFIA-related disorder	HGNC:7784	Homo sapiens (human)	4774	NFIA	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:4483	rhinitis	HGNC:1604	Homo sapiens (human)	1232	CCR3	inference by association of genotype from phenotype used in manual assertion	PMID:17135764
DOID:1312	focal segmental glomerulosclerosis	HGNC:14258	Homo sapiens (human)	23607	CD2AP	inference by association of genotype from phenotype used in manual assertion	PMID:12764198
DOID:0110679	congenital myasthenic syndrome 4C	HGNC:1966	Homo sapiens (human)	1145	CHRNE	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060549	Barber-Say syndrome	HGNC:20670	Homo sapiens (human)	117581	TWIST2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:12365	malaria	HGNC:3618	Homo sapiens (human)	2213	FCGR2B	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:9074	systemic lupus erythematosus	HGNC:11892	Homo sapiens (human)	7124	TNF	inference by association of genotype from phenotype used in manual assertion	PMID:11607787
DOID:2018	hyperinsulinism	HGNC:6081	Homo sapiens (human)	3630	INS	inference by association of genotype from phenotype used in manual assertion	PMID:9667398
DOID:8924	autoimmune thrombocytopenic purpura	HGNC:6001	Homo sapiens (human)	3558	IL2	inference by association of genotype from phenotype used in manual assertion	PMID:20626741
DOID:5844	myocardial infarction	HGNC:6700	Homo sapiens (human)	7804	LRP8	inference by association of genotype from phenotype used in manual assertion	PMID:17847002 RGD:7240710
DOID:0070382	developmental and epileptic encephalopathy 95	HGNC:14937	Homo sapiens (human)	94005	PIGS	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:13223	uterine fibroid	HGNC:29190	Homo sapiens (human)	23112	TNRC6B	inference by association of genotype from phenotype used in manual assertion	PMID:23892540
DOID:10283	prostate cancer	HGNC:7794	Homo sapiens (human)	4790	NFKB1	inference by association of genotype from phenotype used in manual assertion	PMID:26068031 PMID:26788504 PMID:28797847
DOID:11400	pyelonephritis	HGNC:6026	Homo sapiens (human)	3577	CXCR1	inference by association of genotype from phenotype used in manual assertion	PMID:17786197 PMID:22325052
DOID:3748	esophagus squamous cell carcinoma	HGNC:13726	Homo sapiens (human)	58508	KMT2C	inference by association of genotype from phenotype used in manual assertion	PMID:25151357
DOID:0080950	alopecia-mental retardation syndrome 4	HGNC:6708	Homo sapiens (human)	4047	LSS	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:10652	Alzheimer's disease	HGNC:1774	Homo sapiens (human)	1020	CDK5	inference by association of genotype from phenotype used in manual assertion	PMID:15917097
DOID:104	bacterial infectious disease	HGNC:19191	Homo sapiens (human)	81704	DOCK8	inference by association of genotype from phenotype used in manual assertion	PMID:25724123
DOID:399	tuberculosis	HGNC:2621	Homo sapiens (human)	1557	CYP2C19	inference by association of genotype from phenotype used in manual assertion	PMID:27393733
DOID:0111010	cone-rod dystrophy 5	HGNC:21043	Homo sapiens (human)	83394	PITPNM3	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0112346	hereditary spastic paraplegia 83	HGNC:28242	Homo sapiens (human)	84842	HPDL	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:8893	psoriasis	HGNC:6002	Homo sapiens (human)	50604	IL20	inference by association of genotype from phenotype used in manual assertion	PMID:21109726
DOID:1115	sarcoma	HGNC:11998	Homo sapiens (human)	7157	TP53	inference by association of genotype from phenotype used in manual assertion	PMID:31089155
DOID:850	lung disease	HGNC:1516	Homo sapiens (human)	847	CAT	inference by association of genotype from phenotype used in manual assertion	PMID:19897513

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