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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 **9901 - 9925** 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:12858	Huntington's disease	HGNC:4341	Homo sapiens (human)	2752	GLUL	direct assay evidence used in manual assertion	PMID:3159462 PMID:6237280
DOID:13812	adhesions of uterus	RGD:2965	Rattus norvegicus (Norway rat)	25589	Kdr	mutant phenotype evidence used in manual assertion	PMID:31596310
DOID:0080201	Peters plus syndrome	MGI:2685903	Mus musculus (house mouse)	381694	B3glct	author statement supported by traceable reference	PMID:31600785
DOID:535	sleep disorder	MGI:2441738	Mus musculus (house mouse)	319239	Npsr1	author statement supported by traceable reference	PMID:31619542
DOID:854	collagen disease	FB:FBgn0000299	Drosophila melanogaster (fruit fly)	33727	Col4a1	combinatorial experimental and author inference evidence used in manual assertion	PMID:31623094
DOID:3755	antithrombin III deficiency	HGNC:775	Homo sapiens (human)	462	SERPINC1	inference by association of genotype from phenotype used in manual assertion	PMID:3162535 RGD:7240710
DOID:10881	hand, foot and mouth disease	HGNC:9958	Homo sapiens (human)	5972	REN	direct assay evidence used in manual assertion	PMID:31638922
DOID:2559	opiate dependence	HGNC:7956	Homo sapiens (human)	4886	NPY1R	inference by association of genotype from phenotype used in manual assertion	PMID:31689297 PMID:32757697
DOID:9256	colorectal cancer	HGNC:6693	Homo sapiens (human)	53353	LRP1B	inference by association of genotype from phenotype used in manual assertion	PMID:31693169 PMID:33836681
DOID:10933	obsessive-compulsive disorder	RGD:620218	Rattus norvegicus (Norway rat)	81646	Creb1	direct assay evidence used in manual assertion	PMID:31693870
DOID:2754	glycogen storage disease VI	MGI:97829	Mus musculus (house mouse)	110095	Pygl	author statement supported by traceable reference	PMID:31701076
DOID:0110184	Charcot-Marie-Tooth disease type 4J	FB:FBgn0031611	Drosophila melanogaster (fruit fly)	33658	FIG4	combinatorial experimental and curator inference evidence used in manual assertion	PMID:31704059
DOID:2723	dermatitis	HGNC:11892	Homo sapiens (human)	7124	TNF	direct assay evidence used in manual assertion	PMID:3171214
DOID:446	primary hyperaldosteronism	MGI:105061	Mus musculus (house mouse)	12724	Clcn2	author statement supported by traceable reference	PMID:31727896
DOID:684	hepatocellular carcinoma	HGNC:20456	Homo sapiens (human)	84231	TRAF7	mutant phenotype evidence used in manual assertion	PMID:31730901
DOID:1993	rectum cancer	HGNC:2602	Homo sapiens (human)	1591	CYP24A1	inference by association of genotype from phenotype used in manual assertion	PMID:31740231
DOID:5041	esophageal cancer	HGNC:5994	Homo sapiens (human)	7850	IL1R2	inference by association of genotype from phenotype used in manual assertion	PMID:31744444
DOID:0080199	colorectal carcinoma	HGNC:7562	Homo sapiens (human)	4615	MYD88	mutant phenotype evidence used in manual assertion	PMID:31746347
DOID:5419	schizophrenia	MGI:107688	Mus musculus (house mouse)	16569	Kif3b	author statement supported by traceable reference	PMID:31746486
DOID:0080095	myofibrillar myopathy 4	FB:FBgn0265991	Drosophila melanogaster (fruit fly)	36740	Zasp52	combinatorial experimental and curator inference evidence used in manual assertion	PMID:31746737
DOID:2043	hepatitis B	HGNC:8760	Homo sapiens (human)	5133	PDCD1	direct assay evidence used in manual assertion	PMID:31770816
DOID:9970	obesity	HGNC:24678	Homo sapiens (human)	79068	FTO	mutant phenotype evidence used in manual assertion	PMID:31801409
DOID:4914	esophagus adenocarcinoma	HGNC:4567	Homo sapiens (human)	2886	GRB7	direct assay evidence used in manual assertion	PMID:31809243
DOID:3526	cerebral infarction	HGNC:5434	Homo sapiens (human)	3456	IFNB1	inference by association of genotype from phenotype used in manual assertion	PMID:31810024
DOID:1682	congenital heart disease	HGNC:7881	Homo sapiens (human)	4851	NOTCH1	inference by association of genotype from phenotype used in manual assertion	PMID:31813956

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