GlyCosmos Portal

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

Displaying entries **1851 - 1875** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:3457	invasive lobular carcinoma Aliases: Lobular carcinoma Lobular carcinoma of breast Lobular carcinoma of the breast	cdh1	114424	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:4531	mucoepidermoid carcinoma Aliases: MEC	cdh1	114424	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0111649	ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome Aliases: EEM syndrome EEMS ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome	cdh1	114424	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110680	congenital myasthenic syndrome 2C Aliases: CMS2C congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency	Chrnb1	11443	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110681	congenital myasthenic syndrome 2A Aliases: CMS2A congenital myasthenic syndrome 2A slow-channel	Chrnb1	11443	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060684	autosomal dominant nocturnal frontal lobe epilepsy 3 Aliases: ENFL3 nocturnal frontal lobe epilepsy 3	Chrnb2	11444	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060681	autosomal dominant nocturnal frontal lobe epilepsy Aliases: ENFL	Chrnb2	11444	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110666	congenital myasthenic syndrome 3A Aliases: CMS3A congenital myasthenic syndrome 3A, slow-channel	Chrnd	11447	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110665	congenital myasthenic syndrome 3B Aliases: CMS3B congenital myasthenic syndrome 3B, fast-channel	Chrnd	11447	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110664	congenital myasthenic syndrome 3C Aliases: congenital myasthenic syndrome 3C associated with acetylcholine receptor deficiency	Chrnd	11447	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110677	congenital myasthenic syndrome 4B Aliases: CMS4B congenital myasthenic syndrome 4B fast-channel	Chrne	11448	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110679	congenital myasthenic syndrome 4C Aliases: CMS Id CMS1D CMS4C FIM1 congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency congenital myasthenic syndrome type Id familial infantile myasthenia 1	Chrne	11448	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110678	congenital myasthenic syndrome 4A Aliases: CMS Ia1 CMS1A1 CMS4A congenital myasthenic syndrome 4A slow-channel congenital myasthenic syndrometype Ia1	Chrne	11448	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11723	Duchenne muscular dystrophy Aliases: Muscular dystrophy, Duchenne	Cacna1c Cacna1f Cacna1s Ctss Itga7 Nos1 Nos1ap Slc6a5	114493 171148 192363 24239 24598 50654 682930 81008	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060173	Timothy syndrome	Cacna1c Cacna1f Cacna1s	114493 24239 682930	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050534	congenital stationary night blindness Aliases: congenital essential nyctalopia	Cacna1f Gucy2d Trpm1	114493 361586 79222	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110871	congenital stationary night blindness 2A Aliases: congenital stationary night blindness 2A X-linked	Cacna1f	114493	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111007	X-linked cone-rod dystrophy 3 Aliases: CORDX3	Cacna1f	114493	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050630	Aland Island eye disease Aliases: FORSIUS-ERIKSSON TYPE OCULAR ALBINISM Forsius-Eriksson syndrome	Cacna1f	114493	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110677	congenital myasthenic syndrome 4B Aliases: CMS4B congenital myasthenic syndrome 4B fast-channel	CHRNE	1145	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110678	congenital myasthenic syndrome 4A Aliases: CMS Ia1 CMS1A1 CMS4A congenital myasthenic syndrome 4A slow-channel congenital myasthenic syndrometype Ia1	CHRNE	1145	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110679	congenital myasthenic syndrome 4C Aliases: CMS Id CMS1D CMS4C FIM1 congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency congenital myasthenic syndrome type Id familial infantile myasthenia 1	CHRNE	1145	Homo sapiens (human)	Alliance of Genome Resources
DOID:1070	primary open angle glaucoma Aliases: chronic simple glaucoma	Acvr1 Adipoq Adrb2 Bdnf Col6a3 Esr2 Glul Gucy1a1 Lamb2 Mbl2 Mmp1a Myoc Nos3 Ogg1 Pon1 Sod2 Thbs1 Tlr4 Tnf Trp53	11450 11477 11555 12064 12835 13983 14645 16779 17195 17926 18127 18294 18979 20656 21825 21898 21926 22059 60596 83995	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1936	atherosclerosis	Add1 Adipoq Ager Casr Cd36 Cd40 Cd40lg Clu Col4a2 Cpe Csf1 Dab2ip F2 Fas Fcgr2b Fcgr3 Grn Hmgb1 Hnrnpc Hp Hspa1a Itgam Ldlr Mmp1a Mmp2 Ngf Ngfr Nono Nos3 Pdgfd Pecam1 Pla2g7 Pltp Pon1 Pon3 Ptges3 Rbp4 Selp Stat3 Stau1 Vim Wiz	11450 11518 11596 12374 12491 12759 12827 12876 12977 14061 14102 14130 14131 14824 15289 15381 15439 16409 16835 17390 18049 18053 18127 18613 18830 18979 193740 19662 20344 20848 20853 21939 21947 22352 22404 269823 27226 53610 56351 69601 71785 83995	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3454	brain infarction	Adipoq Adnp Aldh2 Atp2b2 Cacna2d1 Calcrl Cd8a Cfh Cfhr4 Ctsb Gpnmb Gzmb H2-Aa Hgf Hmgb1 Hnmt Htr2b Icam1 Igf2 Il15 Il2 Kcnk6 Mmp8 Mmp9 Pdgfb Prcp Rbfox3 Scn7a Tnf Tpcn2	11450 11538 11669 11941 12293 12525 12628 13030 140483 14939 14960 15234 15289 15559 15894 16002 16168 16183 17394 17395 18591 20272 214403 21926 233979 52150 52897 54598 72461 93695	Mus musculus (house mouse)	Alliance of Genome Resources

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