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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 **11326 - 11350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0060395	chromosome 15q24 deletion syndrome Aliases: 15q24 microdeletion syndrome	Sin3a	20466	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110262	cataract 45 Aliases: CTRCT45	Sipa1l3	74206	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111633	congenital sucrase-isomaltase deficiency Aliases: CSID SI deficiency congenital sucrase-isomaltose malabsorption congenital sucrose intolerance disaccharide intolerance	Sis	69983	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111415	trichohepatoenteric syndrome 1 Aliases: THES1	Skic3	218343	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050456	Buruli ulcer disease Aliases: Bairnsdale ulcer Daintree ulcer Mossman ulcer Searl ulcer Searle's ulcer	Slc11a1	18173	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050456	Buruli ulcer disease Aliases: Bairnsdale ulcer Daintree ulcer Mossman ulcer Searl ulcer Searle's ulcer	Slc11a1	316519	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11759	hypochromic anemia Aliases: ANEMIA HYPOCHROMIC	Slc11a2	18174	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11759	hypochromic anemia Aliases: ANEMIA HYPOCHROMIC	Slc11a2	25715	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110142	Bartter disease type 1 Aliases: BARTS1 Bartter syndrome type 1 Bartter syndrome type 1 antenatal hyperprostaglandin E syndrome 1 hypokalemic alkalosis with hypercalciuria 1 antenatal	Slc12a1	20495	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112159	autosomal dominant nonsyndromic deafness 78 Aliases: DFNA78	Slc12a2	20496	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080460	developmental and epileptic encephalopathy 34 Aliases: DEE34 early infantile epileptic encephalopathy 34	Slc12a5	171373	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111315	idiopathic generalized epilepsy 14 Aliases: EIG14	Slc12a5	171373	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080460	developmental and epileptic encephalopathy 34 Aliases: DEE34 early infantile epileptic encephalopathy 34	Slc12a5	57138	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111315	idiopathic generalized epilepsy 14 Aliases: EIG14	Slc12a5	57138	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2477	motor peripheral neuropathy Aliases: HSMN HSMN - Hereditary sensory and motor neuropathy Hereditary motor and sensory neuropathy Peripheral Motor Neuropathy neuropathic muscular atrophy	Slc12a6	107723	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy Aliases: Andermann syndrome Charlevoix disease corpus callosum agenesis-neuronopathy syndrome	Slc12a6	107723	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050667	alcohol-related neurodevelopmental disorder Aliases: ARND static encephalopathy	Slc13a5 Tmcc2	237831 68875	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080453	developmental and epileptic encephalopathy 25 Aliases: DEE25 developmental and epileptic encephalopathy 25, with amelogenesis imperfecta early infantile epileptic encephalopathy 25	Slc13a5	237831	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111668	Kohlschutter-Tonz syndrome Aliases: KTZS Kohlschutter's syndrome amelocerebrohypohidrotic syndrome epilepsy and yellow teeth epilepsy dementia amelogenesis imperfecta epilepsy-dementia-amelogenesis imperfecta syndrome	Slc13a5	237831	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080453	developmental and epileptic encephalopathy 25 Aliases: DEE25 developmental and epileptic encephalopathy 25, with amelogenesis imperfecta early infantile epileptic encephalopathy 25	Slc13a5	266998	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111668	Kohlschutter-Tonz syndrome Aliases: KTZS Kohlschutter's syndrome amelocerebrohypohidrotic syndrome epilepsy and yellow teeth epilepsy dementia amelogenesis imperfecta epilepsy-dementia-amelogenesis imperfecta syndrome	Slc13a5	266998	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050667	alcohol-related neurodevelopmental disorder Aliases: ARND static encephalopathy	Slc13a5	266998	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:5463	cochlear disease	Slc17a8 Tnf	216227 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110555	autosomal dominant nonsyndromic deafness 25 Aliases: DFNA25 autosomal dominant deafness 25	Slc17a8 Trpv4	216227 63873	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9784	trichinosis Aliases: Trichinella spiralis infection	Slc17a8	216227	Mus musculus (house mouse)	Alliance of Genome Resources

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