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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:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome	MGI:1891436	Mus musculus (house mouse)	20371	Foxp3	author statement supported by traceable reference	PMID:11137992 PMID:19661482
DOID:1184	nephrotic syndrome	MGI:1859637	Mus musculus (house mouse)	54631	Nphs1	author statement supported by traceable reference	PMID:11136707 PMID:12039968 PMID:12039988
DOID:12801	mucopolysaccharidosis III	HGNC:7632	Homo sapiens (human)	4669	NAGLU	direct assay evidence used in manual assertion	PMID:11136549
DOID:8398	osteoarthritis	HGNC:7159	Homo sapiens (human)	4322	MMP13	mutant phenotype evidence used in manual assertion	PMID:11134178
DOID:9521	Laron syndrome	MGI:95708	Mus musculus (house mouse)	14600	Ghr	author statement supported by traceable reference	PMID:11133160 PMID:19269870 PMID:9371826
DOID:3526	cerebral infarction	HGNC:9603	Homo sapiens (human)	5740	PTGIS	inference by association of genotype from phenotype used in manual assertion	PMID:11130769 PMID:28108096 PMID:28478978
DOID:10652	Alzheimer's disease	HGNC:11920	Homo sapiens (human)	355	FAS	inference by association of genotype from phenotype used in manual assertion	PMID:11129341
DOID:9352	type 2 diabetes mellitus	HGNC:12519	Homo sapiens (human)	7352	UCP3	inference by association of genotype from phenotype used in manual assertion	PMID:11126413 PMID:18223008 PMID:9769326
DOID:3265	chronic granulomatous disease	HGNC:2578	Homo sapiens (human)	1536	CYBB	inference by association of genotype from phenotype used in manual assertion	PMID:11122248 PMID:8083361
DOID:13258	typhoid fever	HGNC:6709	Homo sapiens (human)	4049	LTA	inference by association of genotype from phenotype used in manual assertion	PMID:11120931
DOID:13258	typhoid fever	HGNC:11892	Homo sapiens (human)	7124	TNF	inference by association of genotype from phenotype used in manual assertion	PMID:11120931
DOID:13258	typhoid fever	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:11120931
DOID:13258	typhoid fever	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:11120931 PMID:25383971
DOID:1485	cystic fibrosis	HGNC:16	Homo sapiens (human)	12	SERPINA3	direct assay evidence used in manual assertion	PMID:11120905
DOID:9970	obesity	HGNC:4241	Homo sapiens (human)	2673	GFPT1	direct assay evidence used in manual assertion	PMID:11118009
DOID:0050453	lissencephaly	HGNC:8574	Homo sapiens (human)	5048	PAFAH1B1	inference by association of genotype from phenotype used in manual assertion	PMID:11115846
DOID:1793	pancreatic cancer	HGNC:11936	Homo sapiens (human)	356	FASLG	direct assay evidence used in manual assertion	PMID:11115536
DOID:1793	pancreatic cancer	HGNC:6407	Homo sapiens (human)	3845	KRAS	direct assay evidence used in manual assertion	PMID:11115351
DOID:8778	Crohn's disease	HGNC:5962	Homo sapiens (human)	3586	IL10	direct assay evidence used in manual assertion	PMID:11113068
DOID:0081082	acute myelomonocytic leukemia	HGNC:4378	Homo sapiens (human)	8833	GMPS	inference by association of genotype from phenotype used in manual assertion	PMID:11110714
DOID:8947	diabetic retinopathy	HGNC:2707	Homo sapiens (human)	1636	ACE	inference by association of genotype from phenotype used in manual assertion	PMID:11106834 PMID:23065222
DOID:12930	dilated cardiomyopathy	HGNC:7577	Homo sapiens (human)	4625	MYH7	inference by association of genotype from phenotype used in manual assertion	PMID:11106718
DOID:11650	bronchopulmonary dysplasia	HGNC:10798	Homo sapiens (human)	653509	SFTPA1	inference by association of genotype from phenotype used in manual assertion	PMID:11105614 PMID:17264398
DOID:3910	lung adenocarcinoma	HGNC:12828	Homo sapiens (human)	7515	XRCC1	inference by association of genotype from phenotype used in manual assertion	PMID:11104903 PMID:20003463
DOID:0050741	alcohol dependence	HGNC:5287	Homo sapiens (human)	3351	HTR1B	inference by association of genotype from phenotype used in manual assertion	PMID:11104852 PMID:12022963 PMID:21172311 PMID:21906503 PMID:22005095

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