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:14789	spondyloepiphyseal dysplasia congenita Aliases: Late Spondyloepiphyseal Dysplasia	Col2a1 Hapln1	25412 29331	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050847	sleep apnea	Lepr Serpine1	24536 24617	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies Aliases: FENIB	Serpine1 Serpine2 Serpini1	116459 24617 29366	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111079	birdshot chorioretinopathy Aliases: BSCR birdshot chorioretinitis birdshot retinochoroiditis birdshot retinochoroidopathy vitiliginous choroiditis	Il2	116562	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:783	end stage renal disease Aliases: end stage renal failure end-stage kidney disease	Abcc2 Abcc3 Acat1 Ace Agtr2 Bdkrb1 C6 Casr Ccl2 Ccr5 Cd40lg Col1a1 Col3a1 Cpt1a Crp Cxcr1 Cxcr2 Cyp1a1 Drd2 Enpp1 Fcgr2al1 Fcgr2b Fgb Gckr Hmgcr Icam1 Il1a Il1rn Irs1 Itgb3 Kl Klk1 Klk1b3 Klk1c10 Klk1c2 Klk1c9 Lcat Lcn2 Lep Lpl Lrp2 Mlxipl Mmp2 Ngf Nos1 Nos3 Nphs1 Olr1 Pgf Plaur Pparg Ptger4 Scap Scarb1 Serpine1 Slc22a2 Slc34a1 Slc9a5 Tgfb1 Tlr4 Tnf Tnfrsf11b Tnfrsf1a Tnfrsf1b Ucp2	117029 140668 140914 156767 170496 171078 192215 24182 24237 24247 24296 24310 24318 24366 24493 24523 24530 24539 24594 24598 24600 24617 24770 24835 24841 25014 25073 25303 25341 25419 25464 25467 25548 25608 25625 25658 25664 25675 25757 289211 29216 29260 292858 292868 29302 29385 29393 29503 301024 310738 498276 50692 54258 54315 59086 60582 64563 81509 81686 83504 84023 84032 84349 85496 94203	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050200	Korean hemorrhagic fever	Il2ra	25704	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:799	varicose veins Aliases: Varix Venous ectasia Venous varices varices	Dll4 Lum Mmp9 Pecam1 Vim	29583 311332 81682 81687 81818	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O Aliases: Charcot-Marie-Tooth neuropathy axonal type 2O autosomal dominant Charcot-Marie-Tooth disease type 2O autosomal dominant axonal Charcot-Marie-Tooth disease type 2O	Dync1h1	29489	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050580	hereditary lymphedema	Angpt2 Calcrl Flt4 Piezo1 Vegfc	114110 114111 25029 361430 89805	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:0112127	HRPT-related hyperuricemia Aliases: HPRT deficiency, grade I HPRT partial deficiency HPRT-related gout HPRT-related hyperuricemia HPRT1 partial deficiency Kelley-Seegmiller syndrome hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency hypoxanthine guanine phosphoribosyltransferase deficiency, grade I hypoxanthine guanine phosphoribosyltransferase partial deficiency	Hprt1	24465	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1475	lymphangioma Aliases: Congenital lymphangioma benign lymphangioma	Flt4 Kdr	114110 25589	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3312	bipolar disorder Aliases: Manic Bipolar Affective disorder Manic Depressive disorder Manic bipolar I disorder bipolar depression bipolar disorder manic phase manic depression manic disorder mixed bipolar disorder	Akt1 Ank3 Atp1a3 Camk2a Ccl2 Chrm2 Chrnb3 Comt Cs Erbb4 Gabra3 Gabra5 Grin2a Grin2b Grn Gsk3b Htr2c L1cam Ncam1 Ngf Ntrk2 Ptgs2 Reln Slc18a1 Slc6a4 Snca Tnfrsf11b	170587 171131 24185 24213 24267 24409 24410 24586 24718 24770 24947 25054 25187 25341 25400 25553 25693 29143 29219 29527 29707 310738 361833 50687 59323 81645 84027	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome Aliases: Berdon syndrome Megacystis microcolon intestinal hypoperistalsis syndrome megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH visceral myopathy	Chrm3	24260	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080421	developmental and epileptic encephalopathy 11 Aliases: DEE11 early infantile epileptic encephalopathy 11	Scn2a	24766	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:12377	spinal muscular atrophy	Atp7a Dpp6 Hexb	24941 29272 294673	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:5577	gastrinoma Aliases: Gastrin Secreting tumor Gastrin cell tumour malignant gastrinoma	Igf1r Met	24553 25718	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112198	spondyloepimetaphyseal dysplasia with joint laxity type 1 Aliases: SEMDJL1 spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures	B3galt6	298690	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10887	lepromatous leprosy Aliases: type L leprosy	C3	24232	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8029	sporadic breast cancer	Esr1 Phb1	24890 25344	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110313	hypertrophic cardiomyopathy 7 Aliases: CMH7 cardiomyopathy, familial hypertrophic 7	Tnni3	29248	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0090018	autosomal dominant familial periodic fever Aliases: FHF FPF TNF receptor associated periodic syndrome TRAPS familial Hibernian fever hibernian fever tumor necrosis factor receptor associated periodic syndrome	Tnfrsf1a	25625	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060230	basal ganglia calcification Aliases: Fahr disease	Pdgfb Pdgfrb Slc20a2	24628 24629 29502	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2527	nephrosis	Ace Angpt1 Angpt2 Ccl7 Cd59b Cx3cl1 Havcr1 Lamb2 Lrp2 Pdpn Vim	24310 25407 25473 286934 287561 29216 54320 81818 89805 89807 89808	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110657	congenital myasthenic syndrome 8 Aliases: CMS8 congenital myasthenic syndrome 8 with pre- and postsynaptic defects congenital myasthenic syndrome due to agrin deficiency	Agrn	25592	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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