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GlyCosmos Diseases

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

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4851 - 4875** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism
DOID:0050328	congenital hypothyroidism	G6pd Ppargc1a	24377 83516	Rattus norvegicus (Norway rat)
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:13628	favism	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:2383	neonatal jaundice Aliases: neonatal hyperbilirubinemia neonatal icterus	G6pd	24377	Rattus norvegicus (Norway rat)
DOID:0050866	oral squamous cell carcinoma Aliases: mouth squamous cell carcinoma	Gapdh Gsk3b Tnf Tp53	24383 24835 24842 84027	Rattus norvegicus (Norway rat)
DOID:3525	middle cerebral artery infarction	Bad Gapdh Gsk3b Has2 Hmgb1 Nampt Ogg1 Parp1 Tnf	24383 24835 25459 25591 25694 297508 64639 81528 84027	Rattus norvegicus (Norway rat)
DOID:3319	lymphangioleiomyomatosis Aliases: lung lymphangioleiomyomatosis lymphangiomyomatosis pulmonary lymphangioleiomyomatosis	Cpt1a Gapdh	24383 25757	Rattus norvegicus (Norway rat)
DOID:0060108	brain glioma Aliases: lower grade glioma	Gapdh	24383	Rattus norvegicus (Norway rat)
DOID:0050827	rheumatic heart disease Aliases: rheumatic carditis	Gapdh	24383	Rattus norvegicus (Norway rat)
DOID:2018	hyperinsulinism Aliases: hyperinsulinemia	Gck Ins1 Ins2 Kcnj11 Lep Lepr Pfkfb1 Rbp4	24385 24505 24506 24536 24638 25608 25703 83535	Rattus norvegicus (Norway rat)
DOID:11714	gestational diabetes Aliases: GDM Gestational diabetes mellitus Maternal gestational diabetes mellitus	Apod Gck Ins1 Ins2 Lep Ogg1 Rbp4	24385 24505 24506 25239 25608 25703 81528	Rattus norvegicus (Norway rat)
DOID:9452	steatotic liver disease Aliases: Fatty change of liver SLD Steatosis of liver alcoholic fatty liver fatty liver disease hepatic lipidosis hepatic steatosis	Dgat2 G6pc1 Gck Htr2a Ins1 Ins2 Lep Ppara Ppargc1a Ucp2	24385 24505 24506 252900 25608 25634 25747 29595 54315 83516	Rattus norvegicus (Norway rat)
DOID:0060639	permanent neonatal diabetes mellitus Aliases: PDMI PNDM permanent diabetes mellitus of infancy	Gck Ins1 Ins2 Kcnj11	24385 24505 24506 83535	Rattus norvegicus (Norway rat)
DOID:0050524	maturity-onset diabetes of the young Aliases: MODY Mason-type diabetes	Gck Ins2 Pdx1	24385 24506 29535	Rattus norvegicus (Norway rat)
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	Chi3l1 Gck Il1rl1 Kl Lepr Nampt Ogg1 Ppara Rbp4 Tlr4 Tnf Tp53	24385 24536 24835 24842 25556 25703 25747 29260 297508 81528 83504 89824	Rattus norvegicus (Norway rat)
DOID:4194	glucose metabolism disease Aliases: disorder of glucose metabolism	Gck Hk1 Hk2 Hk3 Tlr4	24385 25058 25059 25060 29260	Rattus norvegicus (Norway rat)
DOID:9993	hypoglycemia Aliases: Hypoglycaemia	Akt2 Gck	24385 25233	Rattus norvegicus (Norway rat)
DOID:13317	hyperinsulinemic hypoglycemia Aliases: Islet cell hyperplasia nesidioblastosis persistent hyperinsulinemia hypoglycemia of infancy	Gck	24385	Rattus norvegicus (Norway rat)
DOID:0070216	familial hyperinsulinemic hypoglycemia 3 Aliases: HHF3 hyperinsulinemic hypoglycemia due to glucokinase deficiency hyperinsulinism due to glucokinase deficiency	Gck	24385	Rattus norvegicus (Norway rat)
DOID:0111100	maturity-onset diabetes of the young type 2 Aliases: MODY glucokinase-related MODY type 2 MODY2	Gck	24385	Rattus norvegicus (Norway rat)
DOID:0111241	congenital muscular dystrophy-dystroglycanopathy type A5 Aliases: MDDGA5 Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	Fkrp	243853	Mus musculus (house mouse)
DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I Aliases: LGMD2I Limb-girdle muscular dystrophy due to FKRP deficiency MDDGC5 muscular dystrophy limb-girdle type 2I muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5 muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related	Fkrp	243853	Mus musculus (house mouse)
DOID:0110635	muscular dystrophy-dystroglycanopathy type B5 Aliases: FKRP-related congenital muscular dystrophy MDC1C MDDGB5 congenital muscular dystrophy 1C muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5 muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5	Fkrp	243853	Mus musculus (house mouse)

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