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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 **9351 - 9375** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:758	situs inversus Aliases: Complete transposition Laterality sequence situs inversus viscerum	Zic3	22773	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060374	orofaciodigital syndrome IV Aliases: Baraitser-Burn syndrome OFD4	Tctn3	67590	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070197	distal myopathy 1 Aliases: Distal myopathy type 1 Gowers disease Laing distal myopathy Laing early-onset distal myopathy MPD1	Myh7	140781	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12849	autistic disorder Aliases: Kanner's syndrome autism autistic disorder of childhood onset childhood autism infantile autism	Ank2 C4b Ccl2 Cntnap2 Gabra2 Gabra4 Gabra5 Gabrb1 Gabrb2 Gabrr2 Grm8 Grn H2-Eb1 Hspd1 Kcnq3 Kmt2e Lamb1 Mecp2 Met Nf1 Nlgn1 Nlgn3 Ntrk2 Pecam1 Ptchd1 Rapgef4 Reln Shank2 Slc6a4 Slc9a9 Tnf Vldlr	109676 110862 110886 12268 14395 14397 14400 14401 14409 14823 14824 14969 15510 15567 16777 17257 17295 18015 18212 18613 192167 19699 20296 210274 211612 21926 22359 245537 331004 56508 66797 69188	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2602	chondroma Aliases: central Chondroma	Ptpn11	19247	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111861	Meester-Loeys syndrome Aliases: MRLS	Bgn	12111	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090101	lethal congenital glycogen storage disease of heart Aliases: fatal congenital hypertrophic cardiomyopathy due to GSD fatal congenital hypertrophic cardiomyopathy due to glycogenosis fatal congenital nonlysosomal cardiac glycogenosis phosphorylase kinase deficiency of heart	Prkag2 Prkag3	108099 241113	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060248	Simpson-Golabi-Behmel syndrome type 1 Aliases: DGSX Golabi-Rosen syndrome Golabi-Rosen syndrome SGB syndrome Sara Angers syndrome Simpson dysmorphia syndrome X-linked dysplasia gigantism syndrome bulldog syndrome	Gpc3	14734	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112026	non-syndromic X-linked intellectual disability 99 Aliases: MRX99 X-linked mental retardation 99	Usp9x	22284	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12217	Lewy body dementia Aliases: Dementia with Lewy bodies Diffuse Lewy body disease Lewy body disease Senile dementia of the Lewy body type	Anxa5 Chrna4 Chrna7 Elk1 Gba1 Gpr37 Igf1r Igf2 Map2 Nefl Ngfr Pcna Snca Sncb Sncg	104069 11438 11441 11747 13712 14466 14763 16001 16002 17756 18039 18053 18538 20617 20618	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080412	familial adenomatous polyposis 4	Msh3	17686	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4249	Gerstmann-Straussler-Scheinker syndrome Aliases: Gerstmann-Straussler-Scheinker disease PRION DEMENTIA	Prnp	19122	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111780	TARP syndrome Aliases: Pierre Robin sequence-congenital heart defect-talipes syndrome Pierre Robin syndrome-congenital heart defect-talipes syndrome TARPS talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome	Rbm10	236732	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110873	holoprosencephaly 9 Aliases: HPE9 holoprosencephaly with microphthalmia and first branchial arch anomalies pituitary anomalies with holoprosencephaly-like features	Gli2	14633	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1724	duodenal ulcer Aliases: Curling Ulcer Curling's ulcers Stress Ulcer	Cftr Il27 Slc11a2 Stat3 Tfrc Vegfa	12638 18174 20848 22042 22339 246779	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110680	congenital myasthenic syndrome 2C Aliases: CMS2C congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency	Chrnb1	11443	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12799	mucopolysaccharidosis II Aliases: Hunter syndrome Hunter's syndrome MPS II - Hunter syndrome Mucopolysaccharidosis, MPS-II deficiency of iduronate-2-sulphatase	Ids	15931	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090086	hypogonadotropic hypogonadism 6 with or without anosmia	Fgf8	14179	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070209	hereditary lymphedema ID Aliases: LMPH1D	Vegfc	22341	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070043	autosomal dominant intellectual developmental disorder 13 Aliases: MRD13 autosomal dominant mental retardation 13 autosomal dominant non-syndromic intellectual disability 13 mental retardation, autosomal dominant 13, with neuronal migration defects	Dync1h1	13424	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050144	Kartagener syndrome Aliases: Kartagener's syndrome	Dnah11 Dnah5 Dnai1 Drc1 Mbl2 Slit2	110082 13411 17195 20563 381738 68922	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13550	angle-closure glaucoma Aliases: ACG - Angle-closure glaucoma Angle Closure Glaucoma Closed angle glaucoma Narrow cleft glaucoma primary open-angle glaucoma with narrow angles	Hgf Mmp9 Muc5ac Nos3 Tfap2b	15234 17395 17833 18127 21419	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12662	paracoccidioidomycosis Aliases: Mucocutaneous-lymphangitic paracoccidioidomycosis paracoccidioidal mycosis	Cfb H2-Eb1 Il1rl1 Tnf	14962 14969 17082 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060212	amyotrophic lateral sclerosis type 21 Aliases: ALS21	Matr3	17184	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5113	nutritional deficiency disease	Sod1	20655	Mus musculus (house mouse)	Alliance of Genome Resources

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