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GlyCosmos Diseases

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

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1726 - 1750** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:3611	acute retinal necrosis syndrome Aliases: acute retinal necrosis	HLA-B IFNG	3106 3458	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080745	polymyositis	CCR2 CX3CL1 ELN HGF IFNG IL4 MMP9 PMS1 ROBO1 SLIT2 STAT4 TNFRSF1A TNFRSF1B	2006 3082 3458 3565 4318 5378 6091 6376 6775 7132 7133 729230 9353	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112377	muscular dystrophy-dystroglycanopathy type B14 Aliases: MDDGB14 congenital muscular dystrophy GMPPB-related	Gmppb	40599	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0081365	Paget's disease of bone 2 Aliases: Paget disease of bone-2	TNFRSF11A	8792	Homo sapiens (human)	Alliance of Genome Resources
DOID:8725	vascular dementia Aliases: Multi Infarct Dementia multifocal dementia	InR Nmdar1 htl sgg	31248 40665 42160 42549	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050782	Zollinger-Ellison syndrome	daf-2	175410	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070036	autosomal dominant intellectual developmental disorder 6 Aliases: MRD6 autosomal dominant mental retardation 6 autosomal dominant non-syndromic intellectual disability 6	GRIN2B	2904	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080630	B-lymphoblastic leukemia/lymphoma Aliases: B lymphoblastic leukemia/lymphoma B-ALL precursor B lymphoblastic lymphoma/leukemia	F13a1 Tfpi Tp53	24842 29436 60327	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1824	status epilepticus Aliases: Grand mal status	Abcb1b Abcc2 Abcc8 Abcg2 Acan Adam10 Adam9 Ank3 Apod Aqp1 Aqp4 Bax Bdnf Ccl2 Ccr5 Cfl1 Cnr1 Dmd Dpysl2 Gabrb3 Ghsr Gjb6 Gria1 Gria2 Grik1 Grin1 Grin2a Grn Gsk3b Hcn1 Hrh3 Hsd11b1 Hspa1a Idh2 Il6st Kcnc4 Kcnj11 Kcnk3 Mef2c Mmp9 Mtor Nlgn1 Nlgn2 Nr3c1 Nt5e Ntf3 Ogg1 Pgf Plat Plaur Prkcb Ptgs2 Ptprz1 Rela Reln Slc6a8 Slc8a1 Slc8a2 Slc8a3 Sod2 Src Sstr4 Tnf Xrn2	102857 110891 110893 11487 11502 11595 11735 11815 11826 11829 12028 12064 12631 12774 12780 12801 12934 13405 14402 14623 14799 14800 14805 14810 14811 14815 14824 15165 15483 16195 16514 16527 17260 17395 18205 18294 18654 18669 18751 18791 18793 192167 19225 19283 193740 19697 19699 20296 20541 20608 20656 20779 208188 20927 216856 21926 23959 24128 26357 269951 56637 56717 99296 99738	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2938	Epstein-Barr virus infectious disease Aliases: EBV Infection Epstein-Barr virus infection	Cd163 Cd68 Foxp3 Itgb2 Itgb2l	12514 16414 16415 20371 93671	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110342	osteogenesis imperfecta type 13 Aliases: OI13 osteogenesis imperfecta type XIII	BMP1	649	Homo sapiens (human)	Alliance of Genome Resources
DOID:3891	placental insufficiency	Agtr1a Emp2 Epo Grin1 Grin2a Grin2b Itga2 Pdx1 Ppargc1a	11607 13731 13856 14810 14811 14812 16398 18609 19017	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:655	inherited metabolic disorder Aliases: Inborn Errors of Metabolism Metabolic hereditary disorder inborn metabolism disorder	45566 ace-1 ace-2 ace-3	171905 172841 175076 181706	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	erlin1 erlin2	100151163 541490	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:3007	breast ductal carcinoma Aliases: duct carcinoma	Bsg Cd44 Slco1b2 Tnfrsf10b	12215 12505 21933 28253	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9182	pemphigus	Cd40lg Il2	116562 84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1432	blindness Aliases: vision impairment vision loss visual impairment	Aqp4 Atp6v0e Pnpla6 Rpl26 Slc7a14	11829 11974 19941 241919 50767	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1407	anterior uveitis	C3 Ccl2 Ccr5 Cd59b Il1rn Tlr4 Tnf	117029 24232 24770 24835 25407 29260 60582	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10325	silicosis Aliases: Pneumoconiosis due to silicates Silica pneumoconiosis Silicotic fibrosis of lung silicotuberculosis	C3 Ccl7 Cd36 Chia1 Csf2 Ctla4 Egr1 H2-Ab1 Hnrnpa3 Il1rn Kif3a Marco Mmp13 Prkcb Tnf	12266 12477 12491 12981 13653 14961 16181 16568 17167 17386 18751 20306 21926 229279 81600	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111078	tibial muscular dystrophy Aliases: Finnish tibial muscular dystrophy TMD Tardive tibial muscular dystrophy Udd myopathy Udd type distal myopathy distal titinopathy	Ttn	22138	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1754	mitral valve stenosis Aliases: Mitral stenosis	Il10	16153	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050534	congenital stationary night blindness Aliases: congenital essential nyctalopia	Ca-alpha1D	34950	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:7147	ankylosing spondylitis Aliases: Bekhterev syndrome Bekhterev's disease Marie-Strumpell disease	ace	100144634	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0080943	46,XX sex reversal 5	NR2F2	7026	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050564	autosomal dominant nonsyndromic deafness Aliases: autosomal dominant deafness	COL11A1 EPHA10 GREB1L GRHL2 MAP1B PI4KB THOC1 TRRAP USP48	1301 284656 4131 5298 79977 80000 8295 84196 9984	Homo sapiens (human)	Alliance of Genome Resources

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