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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 **10076 - 10100** 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:3328	temporal lobe epilepsy	MGI:1194488	Mus musculus (house mouse)	22348	Slc32a1	author statement supported by traceable reference	PMID:32954490
DOID:3525	middle cerebral artery infarction	HGNC:7656	Homo sapiens (human)	4684	NCAM1	mutant phenotype evidence used in manual assertion	PMID:32962079
DOID:0080768	pyridoxine-dependent epilepsy	MGI:108186	Mus musculus (house mouse)	110695	Aldh7a1	author statement supported by traceable reference	PMID:32969477
DOID:3393	coronary artery disease	HGNC:2548	Homo sapiens (human)	8029	CUBN	inference by association of genotype from phenotype used in manual assertion	PMID:33004870
DOID:1682	congenital heart disease	FB:FBgn0087002	Drosophila melanogaster (fruit fly)	43827	apolpp	combinatorial experimental and author inference evidence used in manual assertion	PMID:33006316
DOID:10140	dry eye syndrome	MGI:106215	Mus musculus (house mouse)	11830	Aqp5	author statement supported by traceable reference	PMID:33013441
DOID:4928	intrahepatic cholangiocarcinoma	HGNC:6693	Homo sapiens (human)	53353	LRP1B	inference by association of genotype from phenotype used in manual assertion	PMID:33014052
DOID:0111442	optic atrophy 9	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	sequence similarity evidence used in manual assertion	PMID:33028849
DOID:0111442	optic atrophy 9	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	mutant phenotype evidence used in manual assertion	PMID:33028849
DOID:684	hepatocellular carcinoma	HGNC:10768	Homo sapiens (human)	23451	SF3B1	mutant phenotype evidence used in manual assertion	PMID:33038489
DOID:1682	congenital heart disease	ZFIN:ZDB-GENE-030131-4714	Danio rerio (zebrafish)	553365	gnptab	author statement supported by traceable reference used in manual assertion	PMID:33055423
DOID:5419	schizophrenia	ZFIN:ZDB-GENE-030616-135	Danio rerio (zebrafish)	403310	cacna1da	curator inference used in manual assertion	PMID:33057948
DOID:14705	Pfeiffer syndrome	HGNC:3689	Homo sapiens (human)	2263	FGFR2	inference by association of genotype from phenotype used in manual assertion	PMID:33074973 PMID:7795583 RGD:7240710
DOID:0050861	colorectal adenocarcinoma	HGNC:3765	Homo sapiens (human)	2322	FLT3	inference by association of genotype from phenotype used in manual assertion	PMID:33075166
DOID:9352	type 2 diabetes mellitus	HGNC:14388	Homo sapiens (human)	51206	GP6	inference by association of genotype from phenotype used in manual assertion	PMID:33076381
DOID:0080547	metabolic dysfunction-associated steatohepatitis	HGNC:5294	Homo sapiens (human)	3357	HTR2B	inference by association of genotype from phenotype used in manual assertion	PMID:33081272
DOID:9452	steatotic liver disease	HGNC:5293	Homo sapiens (human)	3356	HTR2A	inference by association of genotype from phenotype used in manual assertion	PMID:33081272
DOID:9452	steatotic liver disease	HGNC:5294	Homo sapiens (human)	3357	HTR2B	inference by association of genotype from phenotype used in manual assertion	PMID:33081272
DOID:0060212	amyotrophic lateral sclerosis type 21	MGI:1298379	Mus musculus (house mouse)	17184	Matr3	author statement supported by traceable reference	PMID:33082323
DOID:12098	trigeminal neuralgia	MGI:103156	Mus musculus (house mouse)	14405	Gabrg1	author statement supported by traceable reference	PMID:33083721
DOID:9256	colorectal cancer	HGNC:4585	Homo sapiens (human)	2903	GRIN2A	inference by association of genotype from phenotype used in manual assertion	PMID:33106877
DOID:9256	colorectal cancer	HGNC:3595	Homo sapiens (human)	2195	FAT1	inference by association of genotype from phenotype used in manual assertion	PMID:33106877
DOID:3525	middle cerebral artery infarction	RGD:2143	Rattus norvegicus (Norway rat)	25293	Aqp4	mutant phenotype evidence used in manual assertion	PMID:33127515
DOID:10534	stomach cancer	HGNC:20893	Homo sapiens (human)	54880	BCOR	inference by association of genotype from phenotype used in manual assertion	PMID:33145269
DOID:234	colon adenocarcinoma	HGNC:12637	Homo sapiens (human)	7403	KDM6A	direct assay evidence used in manual assertion	PMID:33174323

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