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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 **9926 - 9950** 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:0050848	obstructive sleep apnea	HGNC:7997	Homo sapiens (human)	3084	NRG1	inference by association of genotype from phenotype used in manual assertion	PMID:25325441
DOID:1059	intellectual disability	HGNC:1938	Homo sapiens (human)	1120	CHKB	inference by association of genotype from phenotype used in manual assertion	PMID:21665002
DOID:224	transient cerebral ischemia	RGD:620563	Rattus norvegicus (Norway rat)	116744	Lpar1	direct assay evidence used in manual assertion	PMID:17173873
DOID:9970	obesity	HGNC:24678	Homo sapiens (human)	79068	FTO	mutant phenotype evidence used in manual assertion	PMID:31801409
DOID:9970	obesity	MGI:104993	Mus musculus (house mouse)	16847	Lepr	author statement supported by traceable reference	MGI:3611487 MGI:3778961 MGI:3778962 MGI:3815208 PMID:12136396 PMID:12590922 PMID:12594516 PMID:12885755 PMID:15207242 PMID:15389315 PMID:15685168 PMID:16113078 PMID:16443782 PMID:19015522 PMID:34390703 PMID:6991317 PMID:6993269 PMID:8177042
DOID:2355	anemia	HGNC:10908	Homo sapiens (human)	4891	SLC11A2	inference by association of genotype from phenotype used in manual assertion	PMID:17510944
DOID:8158	complement component 5 deficiency	HGNC:1331	Homo sapiens (human)	727	C5	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:10652	Alzheimer's disease	HGNC:4617	Homo sapiens (human)	2932	GSK3B	inference by association of genotype from phenotype used in manual assertion	PMID:19154537 PMID:24101602
DOID:3393	coronary artery disease	HGNC:13633	Homo sapiens (human)	9370	ADIPOQ	inference by association of genotype from phenotype used in manual assertion	PMID:27218147
DOID:13207	proliferative diabetic retinopathy	HGNC:20893	Homo sapiens (human)	54880	BCOR	direct assay evidence used in manual assertion	PMID:26248552
DOID:10534	stomach cancer	HGNC:3691	Homo sapiens (human)	2264	FGFR4	mutant phenotype evidence used in manual assertion	PMID:26432329 PMID:32973082
DOID:0070484	Legius syndrome	HGNC:20249	Homo sapiens (human)	161742	SPRED1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060246	MASA syndrome	WB:WBGene00004732	Caenorhabditis elegans	177602	sax-7	combinatorial experimental and author inference evidence used in manual assertion	PMID:25488979
DOID:2377	multiple sclerosis	HGNC:8760	Homo sapiens (human)	5133	PDCD1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111694	familial adult myoclonic epilepsy 7	HGNC:16854	Homo sapiens (human)	9693	RAPGEF2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111739	X-linked deafness 1	HGNC:9462	Homo sapiens (human)	5631	PRPS1	inference by association of genotype from phenotype used in manual assertion	PMID:25785835 RGD:7240710
DOID:12716	newborn respiratory distress syndrome	HGNC:10801	Homo sapiens (human)	6439	SFTPB	inference by association of genotype from phenotype used in manual assertion	PMID:11063734 PMID:12424586 PMID:7832777
DOID:4362	cervical cancer	HGNC:10771	Homo sapiens (human)	10262	SF3B4	mutant phenotype evidence used in manual assertion	PMID:35853859
DOID:0081213	autosomal recessive intellectual developmental disorder 50	HGNC:26114	Homo sapiens (human)	80153	EDC3	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:552	pneumonia	HGNC:6000	Homo sapiens (human)	3557	IL1RN	direct assay evidence used in manual assertion	PMID:16369129
DOID:3083	chronic obstructive pulmonary disease	HGNC:11050	Homo sapiens (human)	6532	SLC6A4	inference by association of genotype from phenotype used in manual assertion	PMID:20981038
DOID:13375	temporal arteritis	HGNC:7036	Homo sapiens (human)	4240	MFGE8	direct assay evidence used in manual assertion	PMID:11748647
DOID:0060060	non-Hodgkin lymphoma	HGNC:6819	Homo sapiens (human)	10892	MALT1	inference by association of genotype from phenotype used in manual assertion	PMID:12560219
DOID:2841	asthma	HGNC:5973	Homo sapiens (human)	3596	IL13	inference by association of genotype from phenotype used in manual assertion	PMID:11588017 PMID:15315330 PMID:16024972 PMID:17006604 PMID:17303794 PMID:18341619 PMID:19575932 PMID:19796199 PMID:20198887 PMID:20484924 PMID:23317483 RGD:7240710
DOID:0080855	Parkinsonism	RGD:3684	Rattus norvegicus (Norway rat)	25715	Slc11a2	direct assay evidence used in manual assertion	PMID:20125122

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