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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:9452	steatotic liver disease	HGNC:286	Homo sapiens (human)	154	ADRB2	inference by association of genotype from phenotype used in manual assertion	PMID:11718682
DOID:14503	neuronal ceroid lipofuscinosis	MGI:1860075	Mus musculus (house mouse)	54397	Ppt2	author statement supported by traceable reference	PMID:11717424
DOID:0110731	neuronal ceroid lipofuscinosis 3	MGI:1298204	Mus musculus (house mouse)	19063	Ppt1	author statement supported by traceable reference	PMID:11717424
DOID:231	motor neuron disease	HGNC:11179	Homo sapiens (human)	6647	SOD1	mutant phenotype evidence used in manual assertion	PMID:11717358
DOID:9744	type 1 diabetes mellitus	MGI:107654	Mus musculus (house mouse)	15980	Ifngr2	author statement supported by traceable reference	PMID:11714835
DOID:9744	type 1 diabetes mellitus	MGI:107656	Mus musculus (house mouse)	15978	Ifng	author statement supported by traceable reference	PMID:11714835
DOID:0060730	torsion dystonia 1	WB:WBGene00003870	Caenorhabditis elegans	174433	ooc-5	mutant phenotype evidence used in manual assertion	PMID:11714689
DOID:0060730	torsion dystonia 1	WB:WBGene00003870	Caenorhabditis elegans	174433	ooc-5	combinatorial experimental and author inference evidence used in manual assertion	PMID:11714689
DOID:2841	asthma	HGNC:6015	Homo sapiens (human)	3566	IL4R	inference by association of genotype from phenotype used in manual assertion	PMID:11709756 PMID:12133990 PMID:12940513 PMID:15479272 PMID:17170387 PMID:17586032 PMID:17823973 PMID:18425216 PMID:20868478
DOID:10003	sensorineural hearing loss	HGNC:12762	Homo sapiens (human)	7466	WFS1	inference by association of genotype from phenotype used in manual assertion	PMID:11709537 PMID:12107816 PMID:23595122
DOID:0050560	Walker-Warburg syndrome	HGNC:19139	Homo sapiens (human)	55624	POMGNT1	inference by association of genotype from phenotype used in manual assertion	PMID:11709191 PMID:15236414 PMID:22554691 PMID:23689641
DOID:8947	diabetic retinopathy	HGNC:3327	Homo sapiens (human)	2006	ELN	direct assay evidence used in manual assertion	PMID:11707314
DOID:4247	coronary restenosis	HGNC:6155	Homo sapiens (human)	3689	ITGB2	inference by association of genotype from phenotype used in manual assertion	PMID:11703955
DOID:2920	membranoproliferative glomerulonephritis	RGD:69651	Rattus norvegicus (Norway rat)	81810	Tgfbr2	direct assay evidence used in manual assertion	PMID:11703592
DOID:8778	Crohn's disease	RGD:3029	Rattus norvegicus (Norway rat)	54266	Madcam1	mutant phenotype evidence used in manual assertion	PMID:11703369
DOID:11758	iron deficiency anemia	HGNC:11740	Homo sapiens (human)	7018	TF	inference by association of genotype from phenotype used in manual assertion	PMID:11703331
DOID:10763	hypertension	HGNC:7873	Homo sapiens (human)	4843	NOS2	inference by association of genotype from phenotype used in manual assertion	PMID:11702222
DOID:0080092	myofibrillar myopathy 1	MGI:1344412	Mus musculus (house mouse)	24131	Ldb3	author statement supported by traceable reference	PMID:11696561
DOID:0081337	congenital myopathy	MGI:1344412	Mus musculus (house mouse)	24131	Ldb3	author statement supported by traceable reference	PMID:11696561
DOID:0060224	atrial fibrillation	HGNC:6266	Homo sapiens (human)	3762	KCNJ5	direct assay evidence used in manual assertion	PMID:11693772
DOID:1612	breast cancer	HGNC:3349	Homo sapiens (human)	2022	ENG	mutant phenotype evidence used in manual assertion	PMID:11691802
DOID:1324	lung cancer	HGNC:7155	Homo sapiens (human)	4312	MMP1	inference by association of genotype from phenotype used in manual assertion	PMID:11691799 PMID:15718477 PMID:19963114
DOID:10003	sensorineural hearing loss	HGNC:16035	Homo sapiens (human)	161497	STRC	inference by association of genotype from phenotype used in manual assertion	PMID:11687802
DOID:9351	diabetes mellitus	HGNC:2592	Homo sapiens (human)	1585	CYP11B2	inference by association of genotype from phenotype used in manual assertion	PMID:11687612
DOID:0110266	cataract 9 multiple types	MGI:88515	Mus musculus (house mouse)	12954	Cryaa	author statement supported by traceable reference	PMID:11687536 PMID:18056999 PMID:19619312 PMID:8812430 PMID:9023351

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