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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 **14876 - 14900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0081219	autosomal recessive intellectual developmental disorder 57	mboa-7	181252	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10908	hydrocephalus Aliases: hydrocephalus, X-linked hydrocephalus, nonsyndromic, autosomal recessive	mboat7 pomk	393509 492773	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0081219	autosomal recessive intellectual developmental disorder 57	mboat7	393509	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0081219	autosomal recessive intellectual developmental disorder 57	mboat7.L	495497	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:11981	morbid obesity Aliases: Severe obesity	mc4r	286833	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0080547	metabolic dysfunction-associated steatohepatitis Aliases: MASH NASH non-alcoholic steatohepatitis nonalcoholic steatohepatitis	mc4r	286833	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:2030	anxiety disorder Aliases: anxiety anxiety state	mc4r	286833	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0050429	Hailey-Hailey disease Aliases: BENIGN CHRONIC PEMPHIGUS Pemphigus, Benign Familial	mca-1	177795	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070050	neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language Aliases: MRD20 autosomal dominant mental retardation 20 mental retardation, autosomal dominant 20	mef-2	172732	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060737	junctional epidermolysis bullosa Herlitz type Aliases: Herlitz type epidermolysis bullosa junctionalis Herlitz-Pearson-type epidermolysis bullosa JEB-H JEB-Herlitz type epidermolysis bullosa letalis junctional epidermolysis bullosa generalisata gravis junctional epidermolysis bullosa, Herlitz-Pearson type	mew	32275	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110639	congenital muscular dystrophy due to integrin alpha-7 deficiency Aliases: congenital muscular dystrophy with ITGA7 deficiency congenital muscular dystrophy with integrin alpha-7 deficiency congenital myopathy due to integrin alpha-7 deficiency	mew	32275	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:10907	microcephaly Aliases: Microcephalus microencephaly	mfsd2a	780091	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0070277	primary autosomal recessive microcephaly 15 Aliases: MCPH15 NEDMISBA neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities	mfsd2a	780091	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0070277	primary autosomal recessive microcephaly 15 Aliases: MCPH15 NEDMISBA neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities	mfsd2aa mfsd2ab	445176 492810	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:10907	microcephaly Aliases: Microcephalus microencephaly	mfsd2aa	492810	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110722	neuronal ceroid lipofuscinosis 7 Aliases: CLN7	mfsd8	564342	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110722	neuronal ceroid lipofuscinosis 7 Aliases: CLN7	mfsd8.L	444062	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0070253	congenital disorder of glycosylation type IIa Aliases: Alkuraya syndrome CDG IIa CDG2A CDGIIa CDGS2 carbohydrate-deficient glycoprotein syndrome, type II congenital disorder of glycosylation, type IIa mental retardation, growth retardation, prominent columella, and open mouth	mgat2	100000478	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0070253	congenital disorder of glycosylation type IIa Aliases: Alkuraya syndrome CDG IIa CDG2A CDGIIa CDGS2 carbohydrate-deficient glycoprotein syndrome, type II congenital disorder of glycosylation, type IIa mental retardation, growth retardation, prominent columella, and open mouth	mgat2 mgat2l	100493854 448439	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0070253	congenital disorder of glycosylation type IIa Aliases: Alkuraya syndrome CDG IIa CDG2A CDGIIa CDGS2 carbohydrate-deficient glycoprotein syndrome, type II congenital disorder of glycosylation, type IIa mental retardation, growth retardation, prominent columella, and open mouth	mgat2.L mgat2.S	414590 444674	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110865	congenital stationary night blindness 1B Aliases: CSNB1B autosomal recessive complete congenital stationary night blindness congenital stationary night blindness 1B autosomal recessive	mgl-1	191707	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070473	Zaki syndrome	mig-14	175020	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050888	syndromic intellectual disability	mnb tay	32547 32771	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070037	autosomal dominant intellectual developmental disorder 7 Aliases: DYRK1A syndrome MRD7 autosomal dominant mental retardation 7 autosomal dominant non-syndromic intellectual disability 7	mnb	32771	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060612	abdominal obesity-metabolic syndrome 3	mnb	32771	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources

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