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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 **7876 - 7900** 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:0112312	male infertility due to globozoospermia	MGI:98817	Mus musculus (house mouse)	22027	Hsp90b1	author statement supported by traceable reference	PMID:21208614
DOID:14789	spondyloepiphyseal dysplasia congenita	HGNC:2200	Homo sapiens (human)	1280	COL2A1	inference by association of genotype from phenotype used in manual assertion	PMID:21204228 PMID:23079993 RGD:7240710
DOID:684	hepatocellular carcinoma	HGNC:6866	Homo sapiens (human)	9448	MAP4K4	mutant phenotype evidence used in manual assertion	PMID:21196414 PMID:27010469
DOID:11119	Gilles de la Tourette syndrome	MGI:96969	Mus musculus (house mouse)	17295	Met	author statement supported by traceable reference	PMID:21195751
DOID:0060041	autism spectrum disorder	MGI:96969	Mus musculus (house mouse)	17295	Met	author statement supported by traceable reference	PMID:21195751
DOID:12930	dilated cardiomyopathy	MGI:98352	Mus musculus (house mouse)	20656	Sod2	author statement supported by traceable reference	PMID:21195081
DOID:0060861	microphthalmia with limb anomalies	MGI:1929878	Mus musculus (house mouse)	64075	Smoc1	author statement supported by traceable reference	PMID:21194678 PMID:21750680
DOID:11257	social phobia	HGNC:13830	Homo sapiens (human)	26047	CNTNAP2	inference by association of genotype from phenotype used in manual assertion	PMID:21193173
DOID:4189	mutism	HGNC:13830	Homo sapiens (human)	26047	CNTNAP2	inference by association of genotype from phenotype used in manual assertion	PMID:21193173
DOID:3312	bipolar disorder	HGNC:1963	Homo sapiens (human)	1142	CHRNB3	inference by association of genotype from phenotype used in manual assertion	PMID:21191315
DOID:1591	renovascular hypertension	RGD:2072	Rattus norvegicus (Norway rat)	24182	Agtr2	direct assay evidence used in manual assertion	PMID:21189405
DOID:3068	glioblastoma	HGNC:8976	Homo sapiens (human)	5291	PIK3CB	mutant phenotype evidence used in manual assertion	PMID:21188471
DOID:526	human immunodeficiency virus infectious disease	HGNC:3619	Homo sapiens (human)	2214	FCGR3A	inference by association of genotype from phenotype used in manual assertion	PMID:21187939
DOID:850	lung disease	HGNC:4940	Homo sapiens (human)	3115	HLA-DPB1	inference by association of genotype from phenotype used in manual assertion	PMID:21186201
DOID:1574	alcohol use disorder	HGNC:5302	Homo sapiens (human)	3363	HTR7	inference by association of genotype from phenotype used in manual assertion	PMID:21184583
DOID:326	ischemia	RGD:2254	Rattus norvegicus (Norway rat)	24241	Calca	mutant phenotype evidence used in manual assertion	PMID:21181115
DOID:2986	IgA glomerulonephritis	HGNC:7808	Homo sapiens (human)	4803	NGF	inference by association of genotype from phenotype used in manual assertion	PMID:21178826
DOID:526	human immunodeficiency virus infectious disease	HGNC:11935	Homo sapiens (human)	959	CD40LG	direct assay evidence used in manual assertion	PMID:21177803
DOID:557	kidney disease	WB:WBGene00016848	Caenorhabditis elegans	177557	klo-1	mutant phenotype evidence used in manual assertion	PMID:21177529
DOID:557	kidney disease	WB:WBGene00016848	Caenorhabditis elegans	177557	klo-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:21177529
DOID:2377	multiple sclerosis	HGNC:6953	Homo sapiens (human)	4179	CD46	direct assay evidence used in manual assertion	PMID:21177319
DOID:3526	cerebral infarction	HGNC:9456	Homo sapiens (human)	5627	PROS1	inference by association of genotype from phenotype used in manual assertion	PMID:21172841
DOID:9253	gastrointestinal stromal tumor	HGNC:2433	Homo sapiens (human)	1436	CSF1R	genetic interaction evidence used in manual assertion	PMID:21171987
DOID:2957	pulmonary tuberculosis	HGNC:10907	Homo sapiens (human)	6556	SLC11A1	inference by association of genotype from phenotype used in manual assertion	PMID:21169917 PMID:24024195
DOID:0111816	syndactyly type 1	HGNC:5956	Homo sapiens (human)	3549	IHH	inference by association of genotype from phenotype used in manual assertion	PMID:21167467

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