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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 **11726 - 11750** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:0050718	vitamin metabolic disorder	SLC5A12 SLC5A5 SLC5A6 SLC5A8	159963 160728 6528 8884	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081138	agammaglobulinemia 6	Cd79b	15985	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050750	splenic marginal zone lymphoma	Cd79b	15985	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111995	immunodeficiency 28 Aliases: IFNGR2 deficiency IMD28 MSMD due to complete IFNgammaR2 deficiency MSMD due to complete interferon gamma receptor 2 deficiency Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency immunodeficiency 28, mycobacteriosis	Ifngr2	15980	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111955	immunodeficiency 27A Aliases: IMD27A autosomal recessive IFNGR1 deficiency autosomal recessive MSMD due to partial IFNgammaR1 deficiency autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency autosomal recessive immunodeficiency 27A, mycobacteriosis autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency	Ifngr1	15979	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111956	immunodeficiency 27B Aliases: IMD27B autosomal dominant IFNGR1 deficiency autosomal dominant MSMD due to partial IFNgammaR1 deficiency autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency autosomal dominant immunodeficiency 27B, mycobacteriosis autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency	Ifngr1	15979	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112006	immunodeficiency 69 Aliases: IMD69	Ifng	15978	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9123	eczema herpeticum Aliases: Herpes simplex dermatitis of eyelid Herpes simplex eyelid dermatitis Herpes simplex virus dermatitis herpes simplex dermatitis herpes simplex virus eyelid dermatitis	Ifng	15978	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080325	tuberous sclerosis 2	Ifng	15978	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14176	selective IgG deficiency disease Aliases: Immunoglobin G subclass deficiency Selective IgG Immunodeficiency Selective Immunoglobulin G Subclass deficiency Selective deficiency of IgG Selective immunoglobulin G deficiency	Ifng	15978	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11077	brucellosis Aliases: Maltese fever undulant fever	Cd163 Ifng	15978 93671	Mus musculus (house mouse)	Alliance of Genome Resources
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:1884	viral hepatitis Aliases: Viral hepatitis with hepatic coma animal viral hepatitis human viral hepatitis	Ifng Il2	15978 16183	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11121	pulpitis Aliases: pulp stones	Ifng Il1r1 Tlr4	15978 16177 21898	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2862	glucosephosphate dehydrogenase deficiency Aliases: Glucose-6-phosphate dehydrogenase deficiency deficiency of G-6PD	Ifng Il10 Slc4a1	15978 16153 20533	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111994	immunodeficiency 45 Aliases: IMD45	Ifnar2	15976	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112271	spermatogenic failure 49 Aliases: SPGF98	CFAP58	159686	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070311	oligoasthenoteratozoospermia Aliases: OAT oligoasthenoteratospermia	AGFG1 CFAP58 CFAP61 PPP4C SPATA20	159686 26074 3267 5531 64847	Homo sapiens (human)	Alliance of Genome Resources
DOID:12287	Crimean-Congo hemorrhagic fever Aliases: CHF Congo virus Congo-Crimean Hemorrhagic Fever Crimean hemorrhagic fever	Ifna11 Ifna12 Ifna13 Ifna16 Ifna1 Ifna4 Ifna9	15962 15964 15967 15972 230396 230398 242519	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5052	melioidosis Aliases: Nightcliff gardener's disease Pseudoglanders Whitmore's disease acute and fulminating melioidosis subacute and chronic melioidosis	Ifna11 Ifna12 Ifna13 Ifna16 Ifna1 Ifna4 Ifna9 Plaur Serpinf1 Tlr5 Trem1	15962 15964 15967 15972 18793 20317 230396 230398 242519 53791 58217	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10459	common cold Aliases: Acute viral rhinopharyngitis Nasopharyngitis - acute Nasopharyngitis, acute acute coryza acute nasopharyngitis acute rhinitis rhino-sinusitis	Ifna11 Ifna12 Ifna13 Ifna16 Ifna1 Ifna4 Ifna9 Il10 Il1a Il1rn Tslp	15962 15964 15967 15972 16153 16175 16181 230396 230398 242519 53603	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080886	vitamin D-dependent rickets type 1A	CYP27B1	1594	Homo sapiens (human)	Alliance of Genome Resources
DOID:10609	rickets Aliases: active rickets	CYP27B1 FAM20C	1594 56975	Homo sapiens (human)	Alliance of Genome Resources
DOID:12802	mucopolysaccharidosis I Aliases: Hurler syndrome Hurler-Scheie syndrome Lipochondrodystrophy MPS I - Hurler syndrome Mucopolysaccharidosis, MPS-I Mucopolysaccharidosis, type 1 iduronidase deficiency disease	Idua	15932	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

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