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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 **11051 - 11075** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:0081042	T-cell prolymphocytic leukemia Aliases: Prolymphocytic leukemia, T-cell type T Cell Prolymphocytic Leukemia	JAK3	3718	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H Aliases: LGMD2H limb-girdle muscular dystrophy due to TRIM32 deficiency muscular dystrophy Hutterite type sarcotubular myopathy	tn	37190	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110161	Charcot-Marie-Tooth disease type 2R Aliases: CMT2R Charcot-Marie-Tooth neuropathy type 2R autosomal recessive axonal Charcot-Marie-Tooth disease type 2R	tn	37190	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:1470	major depressive disorder Aliases: clinical depression major depression recurrent major depression single major depressive episode unipolar depression	5-HT1A 5-HT1B ChT Nrx-IV SerT Syn mAChR-A nAChRalpha1 nAChRbeta1 nAChRbeta2 vn	37191 37196 37892 37895 38545 38657 39387 41247 42245 42918 42920	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:809	cocaine abuse	5-HT1A 5-HT1B GluRIA SerT nAChRalpha1 nAChRalpha2 nAChRbeta1 nAChRbeta2 pHCl-2	37191 37196 37895 38545 38742 42918 42919 42920 43703	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:302	substance abuse	5-HT1A 5-HT1B SerT vn	37191 37196 37895 38657	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:14320	generalized anxiety disorder	5-HT1A 5-HT1B SerT	37191 37196 37895	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:8645	subacute delirium	5-HT1A 5-HT1B Ace	37191 37196 41625	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:594	panic disorder Aliases: panic anxiety syndrome	5-HT1A 5-HT1B	37191 37196	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:12995	conduct disorder	5-HT1A 5-HT1B	37191 37196	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070041	autosomal dominant intellectual developmental disorder 11 Aliases: MRD11 autosomal dominant mental retardation 11 autosomal dominant non-syndromic intellectual disability 11	cora	37205	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3565	meningioma Aliases: meningeal neoplasm meningothelial cell tumor neoplasm of the meninges primary Meningeal tumor	cora	37205	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2373	hereditary elliptocytosis Aliases: Congenital elliptocytosis ovalocytosis	cora	37205	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080365	endometrial hyperplasia	CA9 CDC25B JUP KRAS PTK2 SKP2 TFF1	3728 3845 5747 6502 7031 768 994	Homo sapiens (human)	Alliance of Genome Resources
DOID:4603	epidermolytic hyperkeratosis Aliases: Bullous ichthyosiform erythroderma Epidermolytic palmoplantar hyperkeratosis epidermolytic ichthyosis	JUP KRT10 KRT1	3728 3848 3858	Homo sapiens (human)	Alliance of Genome Resources
DOID:3390	palmoplantar keratosis Aliases: Keratosis palmaris et plantaris Palmoplantar Keratoderma palmo-plantar keratodermas	JUP	3728	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110083	arrhythmogenic right ventricular dysplasia 12 Aliases: ARVC12 ARVD12 arrhythmogenic right ventricular cardiomyopathy 12 familial arrhythmogenic right ventricular dysplasia 12	JUP	3728	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080551	Naxos disease	JUP	3728	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090094	hypogonadotropic hypogonadism 1 with or without anosmia Aliases: dysplasia olfactogenitalis of de morsier	ANOS1	3730	Homo sapiens (human)	Alliance of Genome Resources
DOID:3614	Kallmann syndrome Aliases: Hypogonadism with anosmia Kallman syndrome Kallman's syndrome familial hypogonadism with anosmia	ANOS1	3730	Homo sapiens (human)	Alliance of Genome Resources
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	gys1 gys2	373082 394155	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:2747	glycogen storage disease Aliases: glycogenosis	gyg1a gyg1b gys2	373082 406831 415152	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0050987	hypomyelinating leukoencephalopathy	KARS1 VPS11	3735 55823	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110204	Charcot-Marie-Tooth disease recessive intermediate B Aliases: CMTRIB Charcot-Marie-Tooth neuropathy recessive intermediate B RI-CMTB autosomal recessive intermediate Charcot-Marie-Tooth disease type B	KARS1	3735	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110534	autosomal recessive nonsyndromic deafness 89 Aliases: DFNB89 autosomal recessive deafness 89	KARS1	3735	Homo sapiens (human)	Alliance of Genome Resources

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