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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 **5751 - 5775** 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:12930	dilated cardiomyopathy	MGI:104311	Mus musculus (house mouse)	19219	Ptger4	author statement supported by traceable reference	PMID:20008274
DOID:0060041	autism spectrum disorder	WB:WBGene00006412	Caenorhabditis elegans	181484	nlg-1	mutant phenotype evidence used in manual assertion	PMID:20010541 PMID:22723984 PMID:26575289
DOID:0060041	autism spectrum disorder	WB:WBGene00006412	Caenorhabditis elegans	181484	nlg-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:20010541 PMID:22723984 PMID:26575289
DOID:0050589	inflammatory bowel disease	HGNC:914	Homo sapiens (human)	567	B2M	mutant phenotype evidence used in manual assertion	PMID:20015205
DOID:3908	lung non-small cell carcinoma	HGNC:9605	Homo sapiens (human)	5743	PTGS2	inference by association of genotype from phenotype used in manual assertion	PMID:20016751
DOID:7148	rheumatoid arthritis	HGNC:6011	Homo sapiens (human)	3562	IL3	inference by association of genotype from phenotype used in manual assertion	PMID:20018070
DOID:769	neuroblastoma	HGNC:14234	Homo sapiens (human)	64324	NSD1	inference by association of genotype from phenotype used in manual assertion	PMID:20018718
DOID:684	hepatocellular carcinoma	HGNC:6973	Homo sapiens (human)	4193	MDM2	inference by association of genotype from phenotype used in manual assertion	PMID:20019189
DOID:684	hepatocellular carcinoma	HGNC:4886	Homo sapiens (human)	3077	HFE	inference by association of genotype from phenotype used in manual assertion	PMID:20019189
DOID:4552	large cell carcinoma	HGNC:7029	Homo sapiens (human)	4233	MET	direct assay evidence used in manual assertion	PMID:20019837
DOID:850	lung disease	HGNC:3179	Homo sapiens (human)	1909	EDNRA	inference by association of genotype from phenotype used in manual assertion	PMID:20028935
DOID:5844	myocardial infarction	HGNC:24678	Homo sapiens (human)	79068	FTO	inference by association of genotype from phenotype used in manual assertion	PMID:20031593 PMID:26772723
DOID:10763	hypertension	HGNC:24678	Homo sapiens (human)	79068	FTO	inference by association of genotype from phenotype used in manual assertion	PMID:20031594
DOID:3910	lung adenocarcinoma	HGNC:7553	Homo sapiens (human)	4609	MYC	direct assay evidence used in manual assertion	PMID:20033209
DOID:5844	myocardial infarction	HGNC:8744	Homo sapiens (human)	5126	PCSK2	inference by association of genotype from phenotype used in manual assertion	PMID:20036365
DOID:10873	Kuhnt-Junius degeneration	HGNC:9204	Homo sapiens (human)	5444	PON1	inference by association of genotype from phenotype used in manual assertion	PMID:20042177
DOID:0050851	glomerulosclerosis	RGD:2072	Rattus norvegicus (Norway rat)	24182	Agtr2	mutant phenotype evidence used in manual assertion	PMID:20042458
DOID:576	proteinuria	RGD:2070	Rattus norvegicus (Norway rat)	24180	Agtr1a	mutant phenotype evidence used in manual assertion	PMID:20042458
DOID:9256	colorectal cancer	MGI:103038	Mus musculus (house mouse)	20848	Stat3	author statement supported by traceable reference	PMID:20042677
DOID:10591	pre-eclampsia	HGNC:2707	Homo sapiens (human)	1636	ACE	inference by association of genotype from phenotype used in manual assertion	PMID:20044877
DOID:2986	IgA glomerulonephritis	HGNC:11365	Homo sapiens (human)	6775	STAT4	inference by association of genotype from phenotype used in manual assertion	PMID:20045654
DOID:1596	depressive disorder	RGD:2056	Rattus norvegicus (Norway rat)	25083	Adra2a	mutant phenotype evidence used in manual assertion	PMID:20047711
DOID:5844	myocardial infarction	RGD:3673	Rattus norvegicus (Norway rat)	29499	Shh	mutant phenotype evidence used in manual assertion	PMID:20052412
DOID:9352	type 2 diabetes mellitus	RGD:3387	Rattus norvegicus (Norway rat)	65248	Prkaa1	mutant phenotype evidence used in manual assertion	PMID:20054491
DOID:289	endometriosis	RGD:620349	Rattus norvegicus (Norway rat)	29527	Ptgs2	mutant phenotype evidence used in manual assertion	PMID:20056215

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