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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:9111	cutaneous leishmaniasis	HGNC:10907	Homo sapiens (human)	6556	SLC11A1	inference by association of genotype from phenotype used in manual assertion	PMID:20089160
DOID:0110079	Leber congenital amaurosis 8	MGI:2136343	Mus musculus (house mouse)	170788	Crb1	author statement supported by traceable reference	PMID:20089206
DOID:9282	ocular hypertension	HGNC:7155	Homo sapiens (human)	4312	MMP1	mutant phenotype evidence used in manual assertion	PMID:20089869
DOID:1040	chronic lymphocytic leukemia	HGNC:6119	Homo sapiens (human)	3662	IRF4	inference by association of genotype from phenotype used in manual assertion	PMID:20090783 PMID:20123861 PMID:20731705 PMID:21791429
DOID:14330	Parkinson's disease	WB:WBGene00004208	Caenorhabditis elegans	174274	ptc-1	expression pattern evidence used in manual assertion	PMID:20091141
DOID:14330	Parkinson's disease	WB:WBGene00004208	Caenorhabditis elegans	174274	ptc-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:20091141
DOID:10534	stomach cancer	HGNC:6693	Homo sapiens (human)	53353	LRP1B	direct assay evidence used in manual assertion	PMID:20095042
DOID:3263	piebaldism	MGI:96677	Mus musculus (house mouse)	16590	Kit	author statement supported by traceable reference	PMID:20095975
DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L	HGNC:27337	Homo sapiens (human)	203859	ANO5	inference by association of genotype from phenotype used in manual assertion	PMID:20096397 PMID:22742934 PMID:23606453 RGD:7240710
DOID:0070201	Miyoshi muscular dystrophy 3	HGNC:27337	Homo sapiens (human)	203859	ANO5	inference by association of genotype from phenotype used in manual assertion	PMID:20096397 RGD:7240710
DOID:9352	type 2 diabetes mellitus	HGNC:4886	Homo sapiens (human)	3077	HFE	inference by association of genotype from phenotype used in manual assertion	PMID:20097100 PMID:30291871
DOID:11450	allergic cutaneous vasculitis	HGNC:2438	Homo sapiens (human)	1440	CSF3	direct assay evidence used in manual assertion	PMID:20100783
DOID:10825	essential hypertension	HGNC:9642	Homo sapiens (human)	5770	PTPN1	inference by association of genotype from phenotype used in manual assertion	PMID:20101100
DOID:1793	pancreatic cancer	HGNC:79	Homo sapiens (human)	28	ABO	inference by association of genotype from phenotype used in manual assertion	PMID:20103627
DOID:10283	prostate cancer	HGNC:8976	Homo sapiens (human)	5291	PIK3CB	mutant phenotype evidence used in manual assertion	PMID:20103642
DOID:2152	ovary epithelial cancer	HGNC:1604	Homo sapiens (human)	1232	CCR3	inference by association of genotype from phenotype used in manual assertion	PMID:20103664
DOID:1934	dysostosis	MGI:107689	Mus musculus (house mouse)	16568	Kif3a	author statement supported by traceable reference	PMID:20106874
DOID:1686	glaucoma	HGNC:3214	Homo sapiens (human)	1938	EEF2	direct assay evidence used in manual assertion	PMID:20107165
DOID:9282	ocular hypertension	HGNC:7610	Homo sapiens (human)	4653	MYOC	inference by association of genotype from phenotype used in manual assertion	PMID:20107173
DOID:3526	cerebral infarction	HGNC:4814	Homo sapiens (human)	8997	KALRN	inference by association of genotype from phenotype used in manual assertion	PMID:20107840 PMID:25917671 PMID:28706949
DOID:8778	Crohn's disease	HGNC:11364	Homo sapiens (human)	6774	STAT3	inference by association of genotype from phenotype used in manual assertion	PMID:20109474 PMID:22269120
DOID:0060903	thrombosis	RGD:728890	Rattus norvegicus (Norway rat)	302668	Ace2	direct assay evidence used in manual assertion	PMID:20111697
DOID:2957	pulmonary tuberculosis	HGNC:10618	Homo sapiens (human)	6347	CCL2	inference by association of genotype from phenotype used in manual assertion	PMID:20111728
DOID:2986	IgA glomerulonephritis	HGNC:1929	Homo sapiens (human)	1113	CHGA	inference by association of genotype from phenotype used in manual assertion	PMID:20113265
DOID:1324	lung cancer	HGNC:1884	Homo sapiens (human)	1080	CFTR	inference by association of genotype from phenotype used in manual assertion	PMID:20116881

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