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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 **14451 - 14475** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:9074	systemic lupus erythematosus Aliases: Lupus Erythematosus, systemic SLE - Lupus Erythematosus, systemic disseminated lupus erythematosus	SMF3	850721	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:557	kidney disease Aliases: impaired renal function disease nephropathy	YLR001C ZWF1	850687 855480	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11717	neonatal diabetes Aliases: diabetes mellitus syndrome in newborn infant neonatal diabetes mellitus	GLK1	850317	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060309	syndromic X-linked intellectual disability Aliases: syndromic X-linked mental retardation	TAF1	853191	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9477	pulmonary embolism Aliases: pulmonary artery embolism pulmonary embolus	BUD2	853770	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1100	ovarian disease	PAT1	850440	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	HXK1 HXK2	850614 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080985	syndromic X-linked intellectual disorder Lujan-Fryns-type	SRB8	850442	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060704	lymphoproliferative syndrome Aliases: Combined immunodeficiency due to ITK deficiency	SMF3	850721	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080827	human cytomegalovirus infection	PEP4	855949	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	GTB1 VPS1	851807 853870	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0112128	X-linked severe congenital neutropenia Aliases: SCNX XLN	LAS17	854353	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:446	primary hyperaldosteronism Aliases: Cushing syndrome Cushing's syndrome hyperaldosteronism	PEP4	855949	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1485	cystic fibrosis Aliases: CF mucoviscidosis	MNL1 NFT1 STE6 YOR1	853198 853671 853978 856611	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080140	multiple congenital anomalies-hypotonia-seizures syndrome 3 Aliases: M syndrome light fixation seizure syndrome	GPI16	856595	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:0111862	congenital bilateral absence of vas deferens Aliases: CAVD CBAVD congenital bilateral agenesis of vas deferens congenital bilateral aplasia of vas deferens	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:854	collagen disease Aliases: collagen disorder	VPS1	853870	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:0080664	diaphyseal medullary stenosis with malignant fibrous histiocytoma Aliases: Hardcastle syndrome bone dysplasia-medullary fibrosarcoma syndrome diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome	MEU1	850704	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	NTE1 SEY1 VPS1	853870 854336 854943	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111674	intellectual developmental disorder with short stature and behavioral abnormalities Aliases: IDDSSBA	SYT1	856210	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:526	human immunodeficiency virus infectious disease Aliases: HIV infection	RLI1 STE6	851665 853671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12351	alcoholic hepatitis Aliases: acute alcoholic hepatitis acute alcoholic liver disease	STE6	853671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:4194	glucose metabolism disease Aliases: disorder of glucose metabolism	EMI2 HXK1 HXK2	850614 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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