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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources
DisGeNET
Glyco-Disease Genes Database (GDGDB)

Displaying entries **7276 - 7300** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:0110429	dilated cardiomyopathy 1H Aliases: dilated cardiomyopathy with conduction defect	Tnf	21926	Mus musculus (house mouse)
DOID:127	leiomyoma Aliases: leiomyomatous neoplasm leiomyomatous tumor	parp1	560788	Danio rerio (zebrafish)
DOID:0060855	autosomal dominant pseudohypoaldosteronism type 1 Aliases: PHA1A autosomal dominant PHA 1	MRC1	4360	Homo sapiens (human)
DOID:0060350	adenine phosphoribosyltransferase deficiency Aliases: 2,8-dihydroxyadenine urolithiasis APRT deficiency	Aprt	48224	Drosophila melanogaster (fruit fly)
DOID:2560	morphine dependence	ABAT ADH1B ALDH2 COMT CYP2B6 ENO2 EXTL3 FDFT1 GAD1 GAD2 MANEA MDH2 NCAM1 NTNG1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG RGMA SMUG1 UMOD	125 1312 1555 18 2026 2137 217 2222 22854 23583 2571 2572 4191 4684 5290 5291 5293 5294 56963 7369 79694 83666	Homo sapiens (human)
DOID:6741	bilateral breast cancer Aliases: Bilateral breast carcinoma	ABO CRLS1 CYP19A1 GALNT12 PTEN SDHB	1588 28 54675 5728 6390 79695	Homo sapiens (human)
DOID:1116	pertussis Aliases: WC - Whooping cough bordetella infection whooping cough	ACOT7 PIK3CG UMOD	11332 5294 7369	Homo sapiens (human)
DOID:3827	congenital diaphragmatic hernia Aliases: Diaphragmatic Hernia	ndst1	496577	Xenopus tropicalis (tropical clawed frog)
DOID:11721	glycogen storage disease VII Aliases: Glycogen storage disease 7 Glycogen storage disease, type VII Muscle phosphofructokinase deficiency glycogen storage disease type VII phosphofructokinase myopathy	Pfkm	18642	Mus musculus (house mouse)
DOID:0070267	congenital disorder of glycosylation type IIo Aliases: CCDC115-CDG CDG IIo CDG syndrome type IIo CDG2O CDGIIdo Carbohydrate deficient glycoprotein syndrome type IIo Congenital disorder of glycosylation type 2o	CCDC115	84317	Homo sapiens (human)
DOID:0060766	autosomal dominant Robinow syndrome 1 Aliases: DRS1	ACADS AMT ARSA ARSD B4GALT7 BAAT CAT CHPT1 CYP11A1 DAG1 DCN DHDDS FOLR1 GALNT14 GAPDH GCSH GLB1 GLDC GPI HSPG2 KL OGG1 PARP1 PGAM2 PIK3CA PIK3CB PIK3CD PIK3CG PRNP PTEN SGPL1 SMC3 STS TNKS XYLT2	11285 142 1583 1605 1634 2348 2597 2653 2720 2731 275 2821 3339 35 410 412 414 4968 5224 5290 5291 5293 5294 5621 56994 570 5728 64132 79623 79947 847 8658 8879 9126 9365	Homo sapiens (human)
DOID:1289	neurodegenerative disease Aliases: degenerative disease	Prkag2 Prkag3 Sarm1 Tpi1	108099 21991 237868 241113	Mus musculus (house mouse)
DOID:0111108	maturity-onset diabetes of the young type 10 Aliases: MODY10	ins.L ins.S	378695 378696	Xenopus laevis (African clawed frog)
DOID:0050866	oral squamous cell carcinoma Aliases: mouth squamous cell carcinoma	Axn Calr Gapdh1 Gapdh2 sgg	31248 32545 35728 41166 43565	Drosophila melanogaster (fruit fly)
DOID:3459	breast carcinoma Aliases: Mammary carcinoma carcinoma of breast	Eno2	24334	Rattus norvegicus (Norway rat)
DOID:10211	cholelithiasis	ugt1a7 ugt1ab	100384891 406731	Danio rerio (zebrafish)
DOID:0060162	dentatorubral-pallidoluysian atrophy Aliases: DRPLA Haw River Syndrome Naito-Oyanagi disease	ARSA ASAH1 CERS1 EPM2A GAPDH GBA1 NAGLU NEU1 PFKL PRNP TMED9	10715 2597 2629 410 427 4669 4758 5211 54732 5621 7957	Homo sapiens (human)
DOID:3827	congenital diaphragmatic hernia Aliases: Diaphragmatic Hernia	hst-1	177675	Caenorhabditis elegans
DOID:0110881	holoprosencephaly 1 Aliases: HPE1	B3GALNT2 CAT COMT CYP2E1 FIG4 FKRP FKTN GAS1 GMPPB L1CAM LARGE1 LSS MOGS PGAP1 PIGN POMGNT1 POMT1 POMT2	10585 1312 148789 1571 2218 23556 2619 29925 29954 3897 4047 55624 7841 79147 80055 847 9215 9896	Homo sapiens (human)
DOID:9063	Ritter's disease Aliases: Dermatitis exfoliativa neonatorum Pemphigus neonatorum Ritter disease Scalded skin syndrome Staphylococcal scalded skin syndrome Toxic epidermal necrolysis, subcorneal type	EXT1	2131	Homo sapiens (human)
DOID:0060001	withdrawal disorder	Comt Htr2a	24267 29595	Rattus norvegicus (Norway rat)
DOID:0070253	congenital disorder of glycosylation type IIa Aliases: Alkuraya syndrome CDG IIa CDG2A CDGIIa CDGS2 carbohydrate-deficient glycoprotein syndrome, type II congenital disorder of glycosylation, type IIa mental retardation, growth retardation, prominent columella, and open mouth	mgat2	100000478	Danio rerio (zebrafish)
DOID:2679	dysembryoplastic neuroepithelial tumor Aliases: Dysembryoplastic Neuroepithelial neoplasm dysembryoplastic neuroepithelial tumour	Braf	109880	Mus musculus (house mouse)
DOID:0112315	brain small vessel disease 3 Aliases: BSVD3	colgalt1.L colgalt1.S	100125229 495521	Xenopus laevis (African clawed frog)
DOID:0110658	congenital myasthenic syndrome 15 Aliases: CMS15 congenital myasthenic syndrome 15 without tubular aggregates	alg14	450072	Danio rerio (zebrafish)

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