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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 **6001 - 6025** 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:12849	autistic disorder	HGNC:1324	Homo sapiens (human)	721	C4B	inference by association of genotype from phenotype used in manual assertion	PMID:20452682
DOID:0090018	TNF receptor–associated periodic syndrome	MGI:1314884	Mus musculus (house mouse)	21937	Tnfrsf1a	author statement supported by traceable reference	PMID:20457915 PMID:9551933
DOID:3068	glioblastoma	HGNC:8893	Homo sapiens (human)	5228	PGF	direct assay evidence used in manual assertion	PMID:20458050
DOID:3526	cerebral infarction	HGNC:3788	Homo sapiens (human)	2346	FOLH1	inference by association of genotype from phenotype used in manual assertion	PMID:20458436
DOID:3526	cerebral infarction	HGNC:9205	Homo sapiens (human)	5445	PON2	inference by association of genotype from phenotype used in manual assertion	PMID:20458436
DOID:3526	cerebral infarction	HGNC:1550	Homo sapiens (human)	875	CBS	inference by association of genotype from phenotype used in manual assertion	PMID:20458436
DOID:3526	cerebral infarction	HGNC:7468	Homo sapiens (human)	4548	MTR	inference by association of genotype from phenotype used in manual assertion	PMID:20458436
DOID:3526	cerebral infarction	HGNC:12441	Homo sapiens (human)	7298	TYMS	inference by association of genotype from phenotype used in manual assertion	PMID:20458436
DOID:3908	lung non-small cell carcinoma	HGNC:7325	Homo sapiens (human)	4436	MSH2	inference by association of genotype from phenotype used in manual assertion	PMID:20458443 PMID:28093084
DOID:14330	Parkinson's disease	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:20462916
DOID:3083	chronic obstructive pulmonary disease	HGNC:12833	Homo sapiens (human)	7520	XRCC5	inference by association of genotype from phenotype used in manual assertion	PMID:20463177
DOID:0050784	primary progressive multiple sclerosis	HGNC:4601	Homo sapiens (human)	2896	GRN	inference by association of genotype from phenotype used in manual assertion	PMID:20463744
DOID:3525	middle cerebral artery infarction	RGD:2677	Rattus norvegicus (Norway rat)	25453	Gdnf	direct assay evidence used in manual assertion	PMID:20468049
DOID:9675	pulmonary emphysema	RGD:620349	Rattus norvegicus (Norway rat)	29527	Ptgs2	mutant phenotype evidence used in manual assertion	PMID:20472710
DOID:848	arthritis	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:20472930
DOID:848	arthritis	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:20472930
DOID:0050745	diffuse large B-cell lymphoma	HGNC:11919	Homo sapiens (human)	958	CD40	inference by association of genotype from phenotype used in manual assertion	PMID:20473910
DOID:0050873	follicular lymphoma	HGNC:11919	Homo sapiens (human)	958	CD40	inference by association of genotype from phenotype used in manual assertion	PMID:20473910
DOID:10763	hypertension	HGNC:6145	Homo sapiens (human)	3680	ITGA9	inference by association of genotype from phenotype used in manual assertion	PMID:20479155
DOID:11830	myopia	MGI:99402	Mus musculus (house mouse)	11540	Adora2a	author statement supported by traceable reference	PMID:20484596
DOID:11830	myopia	HGNC:7166	Homo sapiens (human)	4313	MMP2	inference by association of genotype from phenotype used in manual assertion	PMID:20484597
DOID:3083	chronic obstructive pulmonary disease	HGNC:51	Homo sapiens (human)	4363	ABCC1	inference by association of genotype from phenotype used in manual assertion	PMID:20487524
DOID:10763	hypertension	RGD:3184	Rattus norvegicus (Norway rat)	24598	Nos1	mutant phenotype evidence used in manual assertion	PMID:20494920
DOID:1073	renal hypertension	HGNC:2622	Homo sapiens (human)	1558	CYP2C8	direct assay evidence used in manual assertion	PMID:20495177
DOID:1073	renal hypertension	HGNC:2634	Homo sapiens (human)	1573	CYP2J2	direct assay evidence used in manual assertion	PMID:20495177

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