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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 **301 - 325** 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:2841	asthma	HGNC:1951	Homo sapiens (human)	1129	CHRM2	inference by association of genotype from phenotype used in manual assertion	PMID:19308904
DOID:5614	eye disease	HGNC:2200	Homo sapiens (human)	1280	COL2A1	inference by association of genotype from phenotype used in manual assertion	PMID:19430638
DOID:2560	morphine dependence	RGD:621531	Rattus norvegicus (Norway rat)	50592	Gria1	mutant phenotype evidence used in manual assertion	PMID:22072679 PMID:25716866 PMID:31863796
DOID:3910	lung adenocarcinoma	HGNC:13726	Homo sapiens (human)	58508	KMT2C	inference by association of genotype from phenotype used in manual assertion	PMID:30821106
DOID:0060020	reticular dysgenesis	HGNC:362	Homo sapiens (human)	204	AK2	inference by association of genotype from phenotype used in manual assertion	PMID:19043416 RGD:7240710
DOID:3525	middle cerebral artery infarction	HGNC:7997	Homo sapiens (human)	3084	NRG1	direct assay evidence used in manual assertion	PMID:20691195 PMID:30206770
DOID:0110786	hereditary spastic paraplegia 35	HGNC:21197	Homo sapiens (human)	79152	FA2H	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080563	congenital disorder of glycosylation Ik	SGD:S000000314	Saccharomyces cerevisiae S288C	852407	ALG1	genetic interaction evidence used in manual assertion	PMID:26931382
DOID:11119	Gilles de la Tourette syndrome	MGI:94862	Mus musculus (house mouse)	13162	Slc6a3	author statement supported by traceable reference	PMID:15710042
DOID:9744	type 1 diabetes mellitus	RGD:2184	Rattus norvegicus (Norway rat)	24221	Avp	inference by association of genotype from phenotype used in manual assertion	PMID:13995944 PMID:5692127
DOID:0060903	thrombosis	HGNC:6137	Homo sapiens (human)	3673	ITGA2	direct assay evidence used in manual assertion	PMID:14563646
DOID:2841	asthma	HGNC:11849	Homo sapiens (human)	7098	TLR3	inference by association of genotype from phenotype used in manual assertion	PMID:17434873
DOID:2734	keratosis follicularis	HGNC:812	Homo sapiens (human)	488	ATP2A2	inference by association of genotype from phenotype used in manual assertion	PMID:10080178 RGD:7240710
DOID:4248	coronary stenosis	HGNC:8823	Homo sapiens (human)	5175	PECAM1	inference by association of genotype from phenotype used in manual assertion	PMID:10571959
DOID:0081007	RNASET2-deficient cystic leukoencephalopathy	ZFIN:ZDB-GENE-030131-2513	Danio rerio (zebrafish)	791890	rnaset2	author statement supported by traceable reference used in manual assertion	PMID:32212285 PMID:32295832
DOID:0070287	primary autosomal recessive microcephaly 11	HGNC:3182	Homo sapiens (human)	1911	PHC1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111584	dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome	HGNC:6636	Homo sapiens (human)	4000	LMNA	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060250	idiopathic scoliosis	MGI:1916151	Mus musculus (house mouse)	215798	Adgrg6	author statement supported by traceable reference	PMID:25954032 PMID:34318745
DOID:848	arthritis	HGNC:19100	Homo sapiens (human)	149233	IL23R	inference by association of genotype from phenotype used in manual assertion	PMID:19035472
DOID:1584	acute chest syndrome	HGNC:7876	Homo sapiens (human)	4846	NOS3	inference by association of genotype from phenotype used in manual assertion	PMID:14687036 PMID:25263931
DOID:0050426	Stevens-Johnson syndrome	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:8841298
DOID:0110495	autosomal recessive nonsyndromic deafness 37	HGNC:7605	Homo sapiens (human)	4646	MYO6	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0112373	autosomal dominant auditory neuropathy 3	HGNC:28472	Homo sapiens (human)	79188	TMEM43	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:1574	alcohol use disorder	RGD:2848	Rattus norvegicus (Norway rat)	25187	Htr2c	direct assay evidence used in manual assertion	PMID:24041931
DOID:684	hepatocellular carcinoma	HGNC:8975	Homo sapiens (human)	5290	PIK3CA	inference by association of genotype from phenotype used in manual assertion	PMID:24673525 PMID:26823876 RGD:7240710

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