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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 **1876 - 1900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:3702	cervical adenocarcinoma Aliases: adenocarcinoma cervix uteri adenocarcinoma of cervix adenocarcinoma of the uterine Cervix	Tfrc Tp53	24842 64678	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:6364	migraine Aliases: migraine disorder migraine variant migraine with or without aura	Cacna1a Calca Cd40lg Ednra Esr1 Htr7 Kcnk18 Nos3 Tnf Trpv1	24241 24326 24600 24835 24890 25398 445371 65032 83810 84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:649	prion disease Aliases: Prion disease pathway Prion protein disease Spongiform Encephalopathy prion induced disorder transmissible spongiform encephalopathy	Cx3cl1	89808	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111537	paroxysmal extreme pain disorder Aliases: PEPD PEXPD familial rectal pain submandibular, ocular and rectal pain with flushing	Scn9a	78956	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070241	primary coenzyme Q10 deficiency 4 Aliases: COQ10D4 SCAR9 coenzyme Q10 deficiency, primary, 4 spinocerebellar ataxia, autosomal recessive 9	Coq8a	360887	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:699	mitochondrial myopathy Aliases: mitochondrial cytopathy	Slc25a4	85333	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070146	hereditary sensory neuropathy type 4 Aliases: hereditary sensory neuropathy type IV insensitivity to pain, congenital, with anhidrosis	Ntrk1	59109	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080228	autosomal dominant intellectual developmental disorder 53 Aliases: autosomal dominant mental retardation 53	Camk2a	25400	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:264	hemangiopericytoma Aliases: Haemangiopericytic meningioma hemangiopericytoma, malignant malignant hemangiopericytoma	Dll4 Kdr Notch1	25496 25589 311332	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10605	short bowel syndrome Aliases: acquired short bowel syndrome short gut syndrome	Clmp Lep Lepr	24536 25608 286939	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111862	congenital bilateral absence of vas deferens Aliases: CAVD CBAVD congenital bilateral agenesis of vas deferens congenital bilateral aplasia of vas deferens	Cftr	24255	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10825	essential hypertension Aliases: idiopathic hypertension primary hypertension	Add1 Agtr1a Agtr1b Atp1b1 Atp5pf Fgfr2 Havcr1 Hsd11b1 Lcn2 Nos3 Npr2 Rbp4 Ren Slc12a3 Timd2	116564 170496 24170 24180 24600 24715 25022 25116 25650 25703 286934 287222 54300 81638 94271	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1936	atherosclerosis	Add1 Agt Casr Cd40lg Clu Cpe Crp Fas Fcgr2a Fcgr2al1 Fcgr2b Grn Hmgb1 Hp Ldlr Mmp2 Ngf Ngfr Nos3 Pdgfd Pecam1 Pon1 Pon3 Ptges3 Rbp4 Selp Vim	116591 24170 24179 24247 24464 24596 24600 246097 24854 25419 25459 25651 25669 25703 289211 29143 29583 300438 310738 312086 362809 498276 66018 81686 81818 84024 84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111258	pentosuria Aliases: L-xylulose reductase deficiency L-xylulosuria PNTSU essential pentosuria xylitol dehydrogenase deficiency	Dcxr	171408	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110290	autosomal recessive limb-girdle muscular dystrophy type 2X Aliases: LGMD2X muscular dystrophy, limb-girdle, type 2X	Bves	365603	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3840	craniopharyngioma Aliases: neoplasm of Rathke's Pouch	Pdgfra	25267	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3388	periodontal disease Aliases: disease of supporting structures of teeth periodontium disorder	Brinp3 Cd40lg Il15 Il21 Il24	170819 25670 286901 365769 84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4166	syphilis Aliases: syphilitic chancre	Ccr5 Kir3dl1 Nefl	117029 353253 83613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9775	diastolic heart failure	Ace Lepr	24310 24536	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1907	malignant fibrous histiocytoma Aliases: Fibroxanthosarcoma MFH	Ppargc1a	83516	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14654	prostatitis	Bambi Ccl11 Il10 Ptgs2	25325 29397 29527 83837	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10126	keratoconus Aliases: conical cornea	Bdnf Hgf Il1a Il1rn Mmp2 Pon1	24225 24446 24493 60582 81686 84024	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060695	hyperekplexia Aliases: Kok disease congenital stiff man syndrome familial startle disease hereditary hyperekplexia startle disease	Glra1	25674	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111252	vestibular schwannomatosis Aliases: ACN BANF NF2 NF2-related schwannomatosis SWN3 SWNV acoustic neurofibromatosis bilateral acoustic neurinoma bilateral acoustic neurofibromatosis bilateral acoustic schwannomas central neurofibromatosis familial acoustic neuromas neurofibromatosis 2 neurofibromatosis type II schwannomatosis 3	Vegfa	83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060246	MASA syndrome Aliases: CRASH syndrome Gareis-Mason syndrome L1 syndrome SPG1 X-linked complicated hereditary spastic paraplegia type 1 X-linked corpus callosum agenesis X-linked spastic paraplegia 1 hereditary spastic paraplegia 1	L1cam Nfasc	116690 50687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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