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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 **13851 - 13875** 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:3565	meningioma	HGNC:12828	Homo sapiens (human)	7515	XRCC1	inference by association of genotype from phenotype used in manual assertion	PMID:18330515
DOID:2339	Crouzon syndrome	HGNC:3689	Homo sapiens (human)	2263	FGFR2	inference by association of genotype from phenotype used in manual assertion	PMID:11380921 PMID:11711827 PMID:7874170 PMID:7987400 RGD:7240710
DOID:0080855	Parkinsonism	RGD:620349	Rattus norvegicus (Norway rat)	29527	Ptgs2	direct assay evidence used in manual assertion	PMID:16781689
DOID:0070150	hereditary sensory and autonomic neuropathy type 2B	HGNC:25964	Homo sapiens (human)	54463	RETREG1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:2596	larynx cancer	HGNC:4553	Homo sapiens (human)	2876	GPX1	inference by association of genotype from phenotype used in manual assertion	PMID:23516596
DOID:1936	atherosclerosis	HGNC:2203	Homo sapiens (human)	1284	COL4A2	inference by association of genotype from phenotype used in manual assertion	PMID:28642624
DOID:0050709	early infantile epileptic encephalopathy	SGD:S000005662	Saccharomyces cerevisiae S288C	854303	IDH2	genetic interaction evidence used in manual assertion	PMID:28058510
DOID:3083	chronic obstructive pulmonary disease	HGNC:4583	Homo sapiens (human)	2901	GRIK5	inference by association of genotype from phenotype used in manual assertion	PMID:28900078
DOID:4029	gastritis	RGD:3645	Rattus norvegicus (Norway rat)	24770	Ccl2	direct assay evidence used in manual assertion	PMID:23892052
DOID:10534	stomach cancer	HGNC:28979	Homo sapiens (human)	23199	GSE1	mutant phenotype evidence used in manual assertion	PMID:29367342
DOID:0060770	dextro-looped transposition of the great arteries	MGI:96257	Mus musculus (house mouse)	15530	Hspg2	author statement supported by traceable reference	PMID:12142349 PMID:12818570
DOID:0111136	congenital generalized lipodystrophy type 2	MGI:1298392	Mus musculus (house mouse)	14705	Bscl2	author statement supported by traceable reference	PMID:21551454 PMID:23680914 PMID:24358199 PMID:24778225
DOID:7693	abdominal aortic aneurysm	RGD:2493	Rattus norvegicus (Norway rat)	24310	Ace	mutant phenotype evidence used in manual assertion	PMID:24602481
DOID:2938	Epstein-Barr virus infectious disease	HGNC:9588	Homo sapiens (human)	5728	PTEN	direct assay evidence used in manual assertion	PMID:19339266
DOID:7693	abdominal aortic aneurysm	RGD:1359376	Rattus norvegicus (Norway rat)	288001	Kng1	inference by association of genotype from phenotype used in manual assertion	PMID:15238617
DOID:0070257	congenital disorder of glycosylation type IIe	HGNC:18622	Homo sapiens (human)	91949	COG7	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:9970	obesity	HGNC:14565	Homo sapiens (human)	10580	SORBS1	inference by association of genotype from phenotype used in manual assertion	PMID:11532984
DOID:5419	schizophrenia	HGNC:4586	Homo sapiens (human)	2904	GRIN2B	direct assay evidence used in manual assertion	PMID:17224684
DOID:162	cancer	SGD:S000003899	Saccharomyces cerevisiae S288C	853603	IML1	genetic interaction evidence used in manual assertion	PMID:23716719
DOID:10584	retinitis pigmentosa	FB:FBgn0002940	Drosophila melanogaster (fruit fly)	42367	ninaE	combinatorial experimental and author inference evidence used in manual assertion	PMID:17170705 PMID:19805114 PMID:20865169 PMID:24553922 PMID:26662796 PMID:27979906 PMID:29425495 PMID:33053617 PMID:33983927 PMID:7708777
DOID:0110652	long QT syndrome 11	HGNC:379	Homo sapiens (human)	10142	AKAP9	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:4531	mucoepidermoid carcinoma	HGNC:1748	Homo sapiens (human)	999	CDH1	direct assay evidence used in manual assertion	PMID:15999364
DOID:5199	ureteral obstruction	RGD:2493	Rattus norvegicus (Norway rat)	24310	Ace	mutant phenotype evidence used in manual assertion	PMID:21667191
DOID:12365	malaria	MGI:107656	Mus musculus (house mouse)	15978	Ifng	author statement supported by traceable reference	PMID:22723523
DOID:2531	hematologic cancer	HGNC:11998	Homo sapiens (human)	7157	TP53	inference by association of genotype from phenotype used in manual assertion	PMID:28387921

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