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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 **451 - 475** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:2237	hepatitis Aliases: acute and subacute liver necrosis acute hepatitis acute/subac. necrosis of liver animal hepatitis chronic hepatitis chronic persistent hepatitis	OGG1	854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2513	basal cell carcinoma Aliases: Basal cell cancer Basal cell carcinoma of skin Basal cell neoplasm Basal cell tumor Epithelioma basal cell Rodent ulcer malignant Basal cell neoplasm malignant basal cell tumor	OGG1	854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12361	Graves' disease Aliases: Grave's disease Graves disease exophthalmic goiter	OGG1	854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5520	head and neck squamous cell carcinoma Aliases: carcinoma of the head and neck squamous cell carcinoma of the head and neck squamous cell carcinomas of head and neck	OGG1	854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1070	primary open angle glaucoma Aliases: chronic simple glaucoma	OGG1	854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9669	senile cataract	GLR1 OGG1	854942 856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070260	congenital disorder of glycosylation type IIh Aliases: CDG IIh CDG2H CDGIIdh COG8-CDG Carbohydrate deficient glycoprotein syndrome type IIh Congenital disorder of glycosylation type 2h	COG8	854904	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060604	ankyloglossia Aliases: tongue-tie	LGR5	8549	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080066	autosomal recessive spinocerebellar ataxia 20 Aliases: SCAR20	MDM1	854867	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110734	neurodegeneration with brain iron accumulation Aliases: NBIA	PAN1	854822	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13359	Ehlers-Danlos syndrome Aliases: Cutis hyperelastica elastic skin	YKE4	854789	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081141	agammaglobulinemia 9	YKE4	854789	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080739	Ehlers-Danlos syndrome spondylodysplastic type 3	YKE4	854789	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10783	methemoglobinemia	CBR1	854768	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060076	estrogen-receptor negative breast cancer	CBR1	854768	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111474	combined oxidative phosphorylation deficiency 1 Aliases: COXPD1 early fatal progressive hepatoencephalopathy hepatoencephalopathy due to COXPD1 hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	GFM1	85476	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070185	X-linked spermatogenic failure 2 Aliases: SPGFX2	SPO22	854737	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0112349	hereditary spastic paraplegia 81 Aliases: SPG81 autosomal recessive complex SPG due to Kennedy pathway dysfunction autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction spastic paraplegia 81 autosomal recessive	SELENOI	85465	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060540	Hermansky-Pudlak syndrome 2	AP3B1	8546	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111077	pyruvate kinase deficiency of red cells Aliases: PK deficiency hemolytic anemia due to red cell pyruvate kinase deficiency pyruvate kinase deficiency of erythrocyte	PYK2	854529	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1926	Gaucher's disease Aliases: Gaucher disease acid beta-glucosidase deficiency glocucerebrosidase deficiency glucosylceramide beta-glucosidase deficiency kerasin thesaurismosis	PYK2	854529	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081441	Nicolaides-Baraitser syndrome Aliases: Intellectual disability-sparse hair-brachydactyly syndrome SPARSE HAIR-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME	SNF2	854465	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050340	opportunistic bacterial infectious disease	SNF2	854465	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081442	blepharophimosis-impaired intellectual development syndrome Aliases: SMARCA2-related blepharophimosis-intellectual disability syndrome	SNF2	854465	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070046	Coffin-Siris syndrome 4 Aliases: CSS4 MRD16 autosomal dominant mental retardation 16	SNF2	854465	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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