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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:1612	breast cancer	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:11349219 PMID:16799707
DOID:10487	Hirschsprung's disease	HGNC:11433	Homo sapiens (human)	6804	STX1A	direct assay evidence used in manual assertion	PMID:11345516
DOID:12177	common variable immunodeficiency	MGI:1858745	Mus musculus (house mouse)	54167	Icos	author statement supported by traceable reference	PMID:11343121 PMID:11343122
DOID:1307	dementia	HGNC:12698	Homo sapiens (human)	7436	VLDLR	inference by association of genotype from phenotype used in manual assertion	PMID:11342683
DOID:6000	congestive heart failure	RGD:621320	Rattus norvegicus (Norway rat)	81687	Mmp9	direct assay evidence used in manual assertion	PMID:11342481
DOID:5082	liver cirrhosis	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:11336748
DOID:5082	liver cirrhosis	HGNC:4948	Homo sapiens (human)	3123	HLA-DRB1	inference by association of genotype from phenotype used in manual assertion	PMID:11336748
DOID:627	severe combined immunodeficiency	HGNC:17642	Homo sapiens (human)	64421	DCLRE1C	inference by association of genotype from phenotype used in manual assertion	PMID:11336668
DOID:3393	coronary artery disease	HGNC:3544	Homo sapiens (human)	2155	F7	inference by association of genotype from phenotype used in manual assertion	PMID:11334615
DOID:9352	type 2 diabetes mellitus	RGD:2689	Rattus norvegicus (Norway rat)	25024	Gipr	inference by association of genotype from phenotype used in manual assertion	PMID:11334402
DOID:0070255	congenital disorder of glycosylation type IIc	HGNC:20197	Homo sapiens (human)	55343	SLC35C1	inference by association of genotype from phenotype used in manual assertion	PMID:11326280 RGD:7240710
DOID:1324	lung cancer	MGI:96680	Mus musculus (house mouse)	16653	Kras	author statement supported by traceable reference	PMID:11323676 PMID:18493606 PMID:20609353 PMID:21512139 PMID:21514245 PMID:24239348 PMID:24430184
DOID:10584	retinitis pigmentosa	RGD:2611	Rattus norvegicus (Norway rat)	25022	Fgfr2	direct assay evidence used in manual assertion	PMID:11319911
DOID:9352	type 2 diabetes mellitus	HGNC:4923	Homo sapiens (human)	3099	HK2	direct assay evidence used in manual assertion	PMID:11319725
DOID:9970	obesity	HGNC:4923	Homo sapiens (human)	3099	HK2	direct assay evidence used in manual assertion	PMID:11319725
DOID:9970	obesity	HGNC:5233	Homo sapiens (human)	3304	HSPA1B	inference by association of genotype from phenotype used in manual assertion	PMID:11319647
DOID:0050851	glomerulosclerosis	RGD:3371	Rattus norvegicus (Norway rat)	25664	Pparg	direct assay evidence used in manual assertion	PMID:11318962
DOID:5419	schizophrenia	HGNC:6051	Homo sapiens (human)	3613	IMPA2	inference by association of genotype from phenotype used in manual assertion	PMID:11317223
DOID:12849	autistic disorder	HGNC:9957	Homo sapiens (human)	5649	RELN	inference by association of genotype from phenotype used in manual assertion	PMID:11317216 PMID:20436377
DOID:2921	glomerulonephritis	RGD:3283	Rattus norvegicus (Norway rat)	24628	Pdgfb	mutant phenotype evidence used in manual assertion	PMID:11316849
DOID:2671	transitional cell carcinoma	HGNC:3690	Homo sapiens (human)	2261	FGFR3	inference by association of genotype from phenotype used in manual assertion	PMID:11314002
DOID:1240	leukemia	HGNC:1014	Homo sapiens (human)	613	BCR	mutant phenotype evidence used in manual assertion	PMID:11313935
DOID:10952	nephritis	RGD:2906	Rattus norvegicus (Norway rat)	29385	Cxcr2	mutant phenotype evidence used in manual assertion	PMID:11313419
DOID:0050638	transthyretin amyloidosis	MGI:98865	Mus musculus (house mouse)	22139	Ttr	author statement supported by traceable reference	PMID:11310831 PMID:29360446
DOID:2018	hyperinsulinism	HGNC:9670	Homo sapiens (human)	5792	PTPRF	direct assay evidence used in manual assertion	PMID:11309481

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