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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 **2626 - 2650** 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:12399	pathological gambling	HGNC:2228	Homo sapiens (human)	1312	COMT	inference by association of genotype from phenotype used in manual assertion	PMID:24390676
DOID:2559	opiate dependence	HGNC:8153	Homo sapiens (human)	4985	OPRD1	inference by association of genotype from phenotype used in manual assertion	PMID:17622222 PMID:22795689 PMID:23612435 PMID:24086514 PMID:24533225 PMID:26233486 PMID:28632076 PMID:28656735 PMID:37531661
DOID:3748	esophagus squamous cell carcinoma	HGNC:7059	Homo sapiens (human)	4255	MGMT	direct assay evidence used in manual assertion	PMID:21674174
DOID:655	inherited metabolic disorder	HGNC:14409	Homo sapiens (human)	60386	SLC25A19	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:3393	coronary artery disease	HGNC:3146	Homo sapiens (human)	1889	ECE1	direct assay evidence used in manual assertion	PMID:10973835
DOID:0080653	urolithiasis	HGNC:9052	Homo sapiens (human)	5328	PLAU	inference by association of genotype from phenotype used in manual assertion	PMID:18240004
DOID:0060075	estrogen-receptor positive breast cancer	HGNC:206	Homo sapiens (human)	10863	ADAM28	direct assay evidence used in manual assertion	PMID:25620615
DOID:1612	breast cancer	HGNC:5960	Homo sapiens (human)	3551	IKBKB	inference by association of genotype from phenotype used in manual assertion	PMID:22562547
DOID:2841	asthma	HGNC:11527	Homo sapiens (human)	6865	TACR2	mutant phenotype evidence used in manual assertion	PMID:19880429
DOID:0060466	gingival fibromatosis	HGNC:11187	Homo sapiens (human)	6654	SOS1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111854	primary ciliary dyskinesia 39	HGNC:25430	Homo sapiens (human)	115399	LRRC56	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060491	SPOAN syndrome	HGNC:20716	Homo sapiens (human)	64837	KLC2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:9821	choroideremia	HGNC:1940	Homo sapiens (human)	1121	CHM	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0110156	Charcot-Marie-Tooth disease type 2B1	HGNC:6636	Homo sapiens (human)	4000	LMNA	inference by association of genotype from phenotype used in manual assertion	PMID:14607793 RGD:7240710
DOID:1793	pancreatic cancer	HGNC:5975	Homo sapiens (human)	3598	IL13RA2	mutant phenotype evidence used in manual assertion	PMID:11748276
DOID:9261	nasopharynx carcinoma	HGNC:4553	Homo sapiens (human)	2876	GPX1	inference by association of genotype from phenotype used in manual assertion	PMID:33616746
DOID:0070409	autosomal recessive spinocerebellar ataxia 28	HGNC:26053	Homo sapiens (human)	54974	THG1L	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:11162	respiratory failure	HGNC:17859	Homo sapiens (human)	23511	NUP188	inference by association of genotype from phenotype used in manual assertion	PMID:32275884
DOID:0050524	maturity-onset diabetes of the young	HGNC:11621	Homo sapiens (human)	6927	HNF1A	inference by association of genotype from phenotype used in manual assertion	PMID:23674172
DOID:9975	cocaine dependence	HGNC:1033	Homo sapiens (human)	627	BDNF	direct assay evidence used in manual assertion	PMID:14973246
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:1614	male breast cancer	HGNC:16627	Homo sapiens (human)	11200	CHEK2	inference by association of genotype from phenotype used in manual assertion	PMID:11967536
DOID:0070029	ITM2B-related cerebral amyloid angiopathy 1	HGNC:6174	Homo sapiens (human)	9445	ITM2B	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050458	juvenile myelomonocytic leukemia	HGNC:7765	Homo sapiens (human)	4763	NF1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:10487	Hirschsprung's disease	MGI:95410	Mus musculus (house mouse)	13866	Erbb2	author statement supported by traceable reference	PMID:12526770

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