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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 **3851 - 3875** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism
DOID:2747	glycogen storage disease Aliases: glycogenosis	C14B9.8 gsy-1 gyg-2 pfk-1.1 pfk-1.2	174924 176149 179335 180119 180583	Caenorhabditis elegans
DOID:1287	cardiovascular system disease Aliases: disease of subdivision of hemolymphoid system	gsy-1	174924	Caenorhabditis elegans
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	gsy-1	174924	Caenorhabditis elegans
DOID:2300	spondylolysis	AGA SLC26A2	175 1836	Homo sapiens (human)
DOID:1949	cholecystitis Aliases: acute and chronic cholecystitis acute cholecystitis acute on chronic cholecystitis chronic cholecystitis	AGA ALDOA ARSA BPGM GGT1 GPI HK1 PKLR PNPLA2 PSAP TPI1	175 226 2678 2821 3098 410 5313 5660 57104 669 7167	Homo sapiens (human)
DOID:13166	allergic bronchopulmonary aspergillosis Aliases: pulmonary aspergillus disease	AGA ALOX15 CAT MBL2 SFTPA1 SFTPA2	175 246 4153 653509 729238 847	Homo sapiens (human)
DOID:9540	vascular skin disease	AGA FUCA1 NEU1 PLAUR PTEN TM7SF2	175 2517 4758 5329 5728 7108	Homo sapiens (human)
DOID:0040099	livedoid vasculitis Aliases: livedoid vasculopathy	AGA FUCA1 NEU1 PTEN	175 2517 4758 5728	Homo sapiens (human)
DOID:8505	dermatitis herpetiformis Aliases: Dermatosis herpetiformis Duhring's disease	AGA ICAM1 SOAT1 TNF	175 3383 6646 7124	Homo sapiens (human)
DOID:1639	skeletal tuberculosis Aliases: osteoarticular tuberculosis	AGA	175	Homo sapiens (human)
DOID:0080484	peroxisome biogenesis disorder 10A Aliases: peroxisome biogenesis disorder 10A (Zellweger)	AGA	175	Homo sapiens (human)
DOID:11371	functional diarrhea Aliases: functional diarrhoea	AGA	175	Homo sapiens (human)
DOID:0111387	familial isolated hypoparathyroidism Aliases: FIH	AGA	175	Homo sapiens (human)
DOID:5212	congenital disorder of glycosylation Aliases: carbohydrate-deficient glycoprotein syndrome	F52B11.2 algn-1 algn-3 bre-4	175065 175920 178364 190668	Caenorhabditis elegans
DOID:0080556	congenital disorder of glycosylation Id Aliases: congenital disorder of glycosylation 1d	algn-3	175065	Caenorhabditis elegans
DOID:1289	neurodegenerative disease Aliases: degenerative disease	tir-1	175502	Caenorhabditis elegans
DOID:332	amyotrophic lateral sclerosis Aliases: ALS Lou Gehrig's disease motor neuron disease, bulbar	tir-1	175502	Caenorhabditis elegans
DOID:0111459	classic galactosemia Aliases: GALT deficiency galactose-1-phosphate uridyltransferase deficiency galactosemia type 1	ZK1058.3	175506	Caenorhabditis elegans
DOID:7998	hyperthyroidism Aliases: overactive thyroid	cts-1 ugt-62	175591 176437	Caenorhabditis elegans
DOID:9744	type 1 diabetes mellitus Aliases: IDDM insulin-dependent diabetes mellitus type I diabetes mellitus	W03G11.3 cht-1 gspd-1 sqv-6 ugt-62	175591 178046 180628 189173 190099	Caenorhabditis elegans
DOID:2741	bilirubin metabolic disorder Aliases: hereditary hyperbilirubinemia hyperbilirubinemia	ugt-61 ugt-62	175591 185500	Caenorhabditis elegans
DOID:3803	Crigler-Najjar syndrome Aliases: Bilirubin UDP glucuronyl transferase deficiency Crigler Najjar syndrome Crigler-Najjar syndrome, type I	ugt-61 ugt-62	175591 185500	Caenorhabditis elegans
DOID:5154	borna disease Aliases: Enzootic encephalomyelitis	aldo-1 aldo-2 parg-1 parg-2 parp-1	175827 176788 177683 186765 266823	Caenorhabditis elegans
DOID:438	autoimmune disease of the nervous system	aldo-1 aldo-2	175827 176788	Caenorhabditis elegans
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	stt-3	175886	Caenorhabditis elegans

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