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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 **201 - 225** 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:0110042	Alzheimer's disease 3	FB:FBgn0284421	Drosophila melanogaster (fruit fly)	40260	Psn	combinatorial experimental and curator inference evidence used in manual assertion	PMID:35654038
DOID:0110042	Alzheimer's disease 3	FB:FBgn0284421	Drosophila melanogaster (fruit fly)	40260	Psn	combinatorial experimental and author inference evidence used in manual assertion	PMID:29790963
DOID:0111364	Alzheimer's disease 9	HGNC:37	Homo sapiens (human)	10347	ABCA7	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:1932	Angelman syndrome	HGNC:12496	Homo sapiens (human)	7337	UBE3A	inference by association of genotype from phenotype used in manual assertion	PMID:8988171 RGD:7240710
DOID:0081289	Antley-Bixler syndrome	HGNC:3689	Homo sapiens (human)	2263	FGFR2	inference by association of genotype from phenotype used in manual assertion	PMID:10633130
DOID:0050462	Antley-Bixler syndrome with disordered steroidogenesis	HGNC:9208	Homo sapiens (human)	5447	POR	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0081290	Antley-Bixler syndrome without disordered steroidogenesis	HGNC:3689	Homo sapiens (human)	2263	FGFR2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070062	Arboleda-Tham syndrome	HGNC:13013	Homo sapiens (human)	7994	KAT6A	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050647	Arts syndrome	HGNC:9005	Homo sapiens (human)	5308	PITX2	inference by association of genotype from phenotype used in manual assertion	PMID:17701896
DOID:0050647	Arts syndrome	HGNC:9462	Homo sapiens (human)	5631	PRPS1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050432	Asperger syndrome	HGNC:10982	Homo sapiens (human)	8604	SLC25A12	inference by association of genotype from phenotype used in manual assertion	PMID:24679184
DOID:14686	Axenfeld-Rieger syndrome	HGNC:9005	Homo sapiens (human)	5308	PITX2	inference by association of genotype from phenotype used in manual assertion	PMID:16876867 PMID:19052653
DOID:14686	Axenfeld-Rieger syndrome	HGNC:3800	Homo sapiens (human)	2296	FOXC1	inference by association of genotype from phenotype used in manual assertion	PMID:12614756 PMID:15477465 PMID:18498376
DOID:0110120	Axenfeld-Rieger syndrome type 1	HGNC:9005	Homo sapiens (human)	5308	PITX2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0110122	Axenfeld-Rieger syndrome type 3	MGI:88180	Mus musculus (house mouse)	12159	Bmp4	author statement supported by traceable reference	PMID:11722794
DOID:0110122	Axenfeld-Rieger syndrome type 3	HGNC:3800	Homo sapiens (human)	2296	FOXC1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:707	B-cell lymphoma	HGNC:1103	Homo sapiens (human)	6046	BRD2	mutant phenotype evidence used in manual assertion	PMID:14563639
DOID:707	B-cell lymphoma	HGNC:74	Homo sapiens (human)	9429	ABCG2	inference by association of genotype from phenotype used in manual assertion	PMID:21918980
DOID:707	B-cell lymphoma	HGNC:1133	Homo sapiens (human)	695	BTK	mutant phenotype evidence used in manual assertion	PMID:28348046
DOID:707	B-cell lymphoma	HGNC:6006	Homo sapiens (human)	50615	IL21R	inference by association of genotype from phenotype used in manual assertion	PMID:11821949
DOID:707	B-cell lymphoma	HGNC:3527	Homo sapiens (human)	2146	EZH2	mutant phenotype evidence used in manual assertion	PMID:29456795
DOID:707	B-cell lymphoma	HGNC:11919	Homo sapiens (human)	958	CD40	mutant phenotype evidence used in manual assertion	PMID:20616215
DOID:707	B-cell lymphoma	MGI:107940	Mus musculus (house mouse)	14056	Ezh2	author statement supported by traceable reference	PMID:27135738
DOID:0080630	B-lymphoblastic leukemia/lymphoma	HGNC:386	Homo sapiens (human)	8644	AKR1C3	direct assay evidence used in manual assertion	PMID:26116659
DOID:0080630	B-lymphoblastic leukemia/lymphoma	HGNC:13176	Homo sapiens (human)	10320	IKZF1	inference by association of genotype from phenotype used in manual assertion	PMID:22699455

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