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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 **6276 - 6300** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:0090027	split hand-foot malformation 2 Aliases: SHFM2	QTRT1 UGT8	7368 81890	Homo sapiens (human)
DOID:0060363	glycerol kinase deficiency	R11F4.1	173747	Caenorhabditis elegans
DOID:13810	familial hypercholesterolemia Aliases: Fredrickson type IIa hyperlipoproteinemia Fredrickson type IIa lipidaemia familial hyperbetalipoproteinaemia familial hypercholesteremia hyperbetalipoproteinemia type II hyperlipidemia	R11F4.1	173747	Caenorhabditis elegans
DOID:653	purine-pyrimidine metabolic disorder Aliases: inborn errors of purine-pyrimidine metabolism	R12E2.11 umps-1	172008 176453	Caenorhabditis elegans
DOID:0050833	orotic aciduria	R12E2.11 umps-1	172008 176453	Caenorhabditis elegans
DOID:0050332	enlarged vestibular aqueduct	RENBP SMUG1	23583 5973	Homo sapiens (human)
DOID:0080566	congenital disorder of glycosylation In Aliases: congenital disorder of glycosylation 1n	RFT1	852261	Saccharomyces cerevisiae S288C
DOID:0080377	peroxisomal biogenesis disorder	RHO1	856294	Saccharomyces cerevisiae S288C
DOID:8577	ulcerative colitis Aliases: Left-sided ulcerative colitis	RHO1	856294	Saccharomyces cerevisiae S288C
DOID:10976	membranous glomerulonephritis Aliases: membranous nephropathy	RHO1	856294	Saccharomyces cerevisiae S288C
DOID:2377	multiple sclerosis Aliases: Generalized multiple sclerosis insular sclerosis	RHO1	856294	Saccharomyces cerevisiae S288C
DOID:9408	acute myocardial infarction	RHO1	856294	Saccharomyces cerevisiae S288C
DOID:0050665	fetal alcohol syndrome	RHO1	856294	Saccharomyces cerevisiae S288C
DOID:4001	ovarian carcinoma	RHO1	856294	Saccharomyces cerevisiae S288C
DOID:0110860	polycystic kidney disease 3 Aliases: Apkd3 Pkd3 Polycystic Kidney Disease, Adult, Type III	ROT2	852530	Saccharomyces cerevisiae S288C
DOID:8465	retinoschisis	RPE	6120	Homo sapiens (human)
DOID:0060746	basal laminar drusen Aliases: cuticular drusen drusen of bruch membrane early adult-onset grouped drusen	RPE	6120	Homo sapiens (human)
DOID:0110016	Leber congenital amaurosis 2 Aliases: LCA2 amaurosis congenita of Leber II	RPE	6120	Homo sapiens (human)
DOID:12165	retinal lattice degeneration Aliases: Palisade degeneration of retina	RPE	6120	Homo sapiens (human)
DOID:0060745	Doyne honeycomb retinal dystrophy Aliases: DHRD Doyne honeycomb degeneration of retina	RPE	6120	Homo sapiens (human)
DOID:0090114	Sorsby's fundus dystrophy Aliases: SFD hemorrhagic macular dystrophy pseudoinflammatory fundus dystrophy of Sorsby	RPE	6120	Homo sapiens (human)
DOID:0111239	congenital muscular dystrophy-dystroglycanopathy type A10 Aliases: MDDGA10 Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10	RXYLT1	10329	Homo sapiens (human)
DOID:11713	diabetic angiopathy Aliases: Diabetic vascular disorder diabetic peripheral angiopathy	Rbp4 Tnf	19662 21926	Mus musculus (house mouse)
DOID:0050912	colon adenoma	Rbp4	19662	Mus musculus (house mouse)
DOID:10825	essential hypertension Aliases: idiopathic hypertension primary hypertension	Rbp4	19662	Mus musculus (house mouse)

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