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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 **9301 - 9325** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	Ifng Tlr2 Tlr4	15978 21898 24088	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080732	Ehlers-Danlos syndrome classic-like 2	Aebp1	11568	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14283	primary hypertrophic osteoarthropathy Aliases: Pachydermoperiostosis of nail Pachydermoperiostosis syndrome	Slco2a1	24059	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5603	T-cell acute lymphoblastic leukemia Aliases: Precursor T Lymphoblastic Leukemia T Acute Lymphoblastic Leukemia T-cell acute lymphocytic leukaemia T-cell leukemia T-cell lymphoblastic leukemia/lymphoma acute T cell leukemia precursor T-lymphoblastic lymphoma/leukemia	Cxcr4 Lyl1 Nup98 Pdgfra	12767 17095 18595 269966	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110827	Usher syndrome type 2 Aliases: USH2	Ush2a	22283	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060717	autosomal recessive congenital ichthyosis 8 Aliases: ARCI8 lamellar ichthyosis 4 late-onset lamellar ichthyosis	Lipn	70166	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111346	epidermolysis bullosa simplex with mottled pigmentation Aliases: EBSMP Epidermolysis bullosa simplex-MP speckled hyperpigmentation with punctate palmoplantar keratoses and childhood blistering	Krt5	110308	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10300	Raynaud disease Aliases: Raynaud's disease Raynaud's syndrome	Hnrnpk	15387	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112146	retinitis pigmentosa 89 Aliases: RP89	Kif3b	16569	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions	Grn	14824	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11400	pyelonephritis	Ace Ambp Bmp7 Calca Cfb Cxcr1 Il1rn Il3 Pgf Tlr1	11421 11699 12162 12310 14962 16181 16187 18654 21897 227288	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1852	intrahepatic cholestasis Aliases: neonatal intrahepatic cholestasis	Abcb11 Abcb4 Entpd1 Slc22a1 Slc22a2 Slc25a13	12495 18670 20517 20518 27413 50799	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110340	osteogenesis imperfecta type 4 Aliases: OI4 osteogenesis imperfecta type IV osteogenesis imperfecta with normal sclera	Col1a1 Col1a2	12842 12843	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081346	congenital myopathy 14	Myl1	17901	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081267	graft-versus-host disease Aliases: GvHD graft versus host disease	Abo Adipoq Ctla4 F3 Fas Fasl Fcgr4 Foxp3 H2-D1 H2-K1 H2-Q10 H2-Q1 H2-Q4 H2-Q6 H2-Q8 Hgf Hspa1a Hspa8 Ifng Il10 Il10rb Il1a Il1rn Il2 Mki67 Pdgfb Sell Tfpi Trp53 Vegfa	110557 11450 12477 14066 14102 14103 14964 14972 15006 15007 15015 15234 15481 15978 16153 16155 16175 16181 16183 17345 18591 193740 20343 20371 21788 22059 22339 246256 68395 80908	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070266	congenital disorder of glycosylation type IIn Aliases: CDG IIn CDG syndrome type IIn CDG2N CDGIIdn Carbohydrate deficient glycoprotein syndrome type IIn Congenital disorder of glycosylation type 2n SLC39A8-CDG	Slc39a8	67547	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070433	hyperphosphatasia with impaired intellectual development syndrome 1 Aliases: GPIBD2 HPMRS1 glycosylphosphatidylinositol biosynthesis defect 2 hyperphosphatasia with mental retardation syndrome 1	Pigv	230801	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081345	congenital myopathy 10B	Megf10	70417	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1827	idiopathic generalized epilepsy Aliases: Generalised epilepsy	Dnm1 Gabra1 Hcn4 Kcnma1	13429 14394 16531 330953	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112063	X-Linked immunodeficiency 74 Aliases: IMD74 TLR7 deficiency X-linked immunodeficiency 74,COVID-19-related respiratory insufficiency due to SARS-CoV-2 viral infection	Tlr7	170743	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3308	embryonal carcinoma Aliases: primary extragonadal embryonal carcinoma	Afp Fgf8 Inha Pou5f1	11576 14179 16322 18999	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14118	familial lipoprotein lipase deficiency Aliases: Fredrickson type I hyperlipoproteinemia Fredrickson type I lipaemia familial LPL deficiency familial hyperlipoproteinemia type I hypercholesterinaemic xanthomatosis hyperchylomicronemia mixed hyperglyceridemia	Lpl	16956	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111390	mucopolysaccharidosis Ih Aliases: Dysostosis multiplex syndrome Hurler disease MPS type 1H Hurler-Pfaundler syndrome L-iduronidase deficiency, Hurler type MPS1-H Mucopolysaccharidosis type I severe form dysostosis multiplex gargoylism	Idua	15932	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070443	neurodevelopmental disorder with cerebellar atrophy and motor dysfunction	Gemin5	216766	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070307	craniolenticulosutural dysplasia Aliases: Boyadjiev-Jabs Syndrome cranio-lenticulo-sutural dysplasia, CLSD	Sec23a Sec23b	20334 27054	Mus musculus (house mouse)	Alliance of Genome Resources

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