GlyCosmos Portal

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

Displaying entries **4076 - 4100** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:6000	congestive heart failure Aliases: CHF Cardiac Failure Congestive Congestive heart disease Weak heart	Acan Ace2 Ace Adam17 Adra2c Adrb1 Adrb3 Agt Agtr1a Agtr2 Aoc3 Casq2 Ccl2 Cd40lg Chi3l1 Chrm4 Chrna4 Corin Creb1 Cs Cst3 Cxcr4 Cyp1a2 Epo Erbb4 Fas Faslg Hmgb1 Hp Htr2a Htr2b Il10 Inhba Kcne1 Kcnk2 Lepr Ltbp2 Mas1 Mdh2 Mme Mmp2 Mmp8 Mmp9 Mstn Ncam1 Nfe2l2 Ngfr Nos1 Nos1ap Nos3 Ogt Oprk1 P2rx4 Parp1 Pgf Plcd1 Pln Ppargc1a Ppp1cc Prkcb Ramp2 Rbp4 Ren Ryr2 Scn5a Scn8a Selp Slc22a5 Slc2a4 Slc6a4 Slc8a1 Sod2 Sox2 Th Timp1 Tnf Tnfrsf11b Tnfrsf1b Ucp2	116510 156767 170587 170899 192363 24175 24179 24180 24182 24297 24310 24335 24464 24536 24586 24590 24596 24598 24600 246097 24655 24669 24715 24770 24787 24835 24925 25023 25085 25111 25139 25153 25307 25325 25341 25385 25459 25471 25553 25590 25591 25645 25651 25665 25703 26295 289596 29152 29200 29209 29335 29473 29581 29595 29659 29710 29715 29726 302668 499593 54315 57027 58966 58968 59106 59323 60628 63849 64672 689560 81646 81686 81687 81829 83516 83619 84349 89824 94203	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081144	common variable immunodeficiency 1	Icos	64545	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9206	Barrett's esophagus Aliases: Barrett esophagus Barrett's esophagus with esophagitis Barrett's oesophagus Barrett's ulcer of esophagus Barretts syndrome ulcerative esophagitis	B3gat2 Cthrc1 Fas Igfbp3 Mmp12 Ptgs2 Smo	117033 24484 246097 25273 282836 29527 64544	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:627	severe combined immunodeficiency Aliases: SCID combined T and B cell inborn immunodeficiency	Cd3d Il2 Ptprc	116562 24699 25710	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9123	eczema herpeticum Aliases: Herpes simplex dermatitis of eyelid Herpes simplex eyelid dermatitis Herpes simplex virus dermatitis herpes simplex dermatitis herpes simplex virus eyelid dermatitis	Ifng	25712	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13636	Fanconi anemia Aliases: Fanconi anaemia Fanconi pancytopenia Fanconi panmyelopathy Fanconi's anaemia Fanconi's anemia	Ifng Il10 Tnf	24835 25325 25712	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110119	autoimmune lymphoproliferative syndrome type 3 Aliases: ALPS3 autoimmune lymphoproliferative syndrome type III	Prkcd	170538	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110317	hypertrophic cardiomyopathy 11 Aliases: CMH11 cardiomyopathy familial hypertrophic 11	Actb Actc1	29275 81822	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:326	ischemia	Akt2 Angpt2 Calca Ccl2 Crhr2 Cx3cl1 Dll4 Htr1b Scnn1a Scnn1b Scnn1g Tnfrsf1a Tp53	24241 24767 24768 24770 24842 25075 25122 25233 25625 311332 64680 89805 89808	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081290	Antley-Bixler syndrome without disordered steroidogenesis	Fgfr2	25022	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060643	primary sclerosing cholangitis	Abcb4 Cftr Dnase1 Gnrhr Krt18 Tnf Vegfa	24255 24835 24891 25633 294853 81668 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1063	interstitial nephritis Aliases: renal tubulo-interstitial disease	Ccl11 Ccl7 Crp	25419 287561 29397	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10016	multiple endocrine neoplasia type 2B Aliases: MEN type IIB MEN2B Multiple endocrine neoplasia, type 3 Wagenmann-Froboese syndrome mucosal neuroma syndrome	Ret	24716	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050419	complement factor I deficiency Aliases: C3 INACTIVATOR DEFICIENCY COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY	Cfi	79126	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:12577	urethral obstruction Aliases: Obstruction of urethra	Nos1 Tgfb1	24598 59086	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050811	congenital adrenal hyperplasia Aliases: adrenal hyperplasia 1 congenital lipoid adrenal hyperplasia lipoid CAH	Ren	24715	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	Atp7a Hmgcr	24941 25675	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4586	familial meningioma	Pdgfb	24628	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080560	congenital disorder of glycosylation Ih Aliases: congenital disorder of glycosylation 1h	Alg8	293129	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:916	liver benign neoplasm Aliases: epithelial hepatic and intrahepatic bile duct neoplasm	Col1a1 Il10 Met	24553 25325 29393	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1555	urticaria	Bdnf Ccr5 Crp Ngfr Sod2	117029 24225 24596 24787 25419	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080470	developmental and epileptic encephalopathy 36 Aliases: congenital disorder of glycosylation, type Is early infantile epileptic encephalopathy 36	Alg13l1	300284	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111876	linear skin defects with multiple congenital anomalies 3 Aliases: LSDMCA3 linear skin defects with cardiomyopathy and other congenital anomalies	Ndufb11	299310	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2600	laryngeal carcinoma Aliases: cancer of larynx carcinoma of larynx	Ackr3 Cxcr4	60628 84348	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:77	gastrointestinal system disease Aliases: GIT disease Gastroenteropathy alimentary system disease digestive system disorder gastrointestinal disease gastrointestinal disorder	Igf2 Mecp2 Tf Vcam1	24483 24825 25361 29386	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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