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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 **4901 - 4925** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:14320	generalized anxiety disorder	5-HT1A 5-HT1B SerT	37191 37196 37895	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: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: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: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: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: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:14566	disease of cellular proliferation Aliases: cell process disease neoplasm	ATM FZR1 JAK1 JAK3 PLAUR SNRPB2 SPP1 TFPI TP53 TYK2	3716 3718 472 51343 5329 6629 6696 7035 7157 7297	Homo sapiens (human)	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	AKR1C3 CARD11 CXCR4 JAK1 JAK3 NBN NUP98 PDGFRA	3716 3718 4683 4928 5156 7852 84433 8644	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060603	isolated anhidrosis with normal sweat glands Aliases: Dann-Epstein-Sohar syndrome	ITPR2	3709	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050978	spinocerebellar ataxia type 29	ITPR1	3708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050965	spinocerebellar ataxia type 15 Aliases: spinocerebellar ataxia type 16	ITPR1	3708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111578	Gillespie syndrome Aliases: GLSP aniridia, cerebellar ataxia and mental deficiency aniridia-cerebellar ataxia-intellectual disability syndrome	ITPR1	3708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070516	Mitchell syndrome	ACOX1	37028	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050797	peroxisomal acyl-CoA oxidase deficiency Aliases: Peroxisomal acyl-coenzyme A oxidase	ACOX1	37028	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060284	paroxysmal nocturnal hemoglobinuria	PIG-A	37020	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2 Aliases: developmental and epileptic encephalopathy 20 early infantile epileptic encephalopathy 20 glycosylphosphatidylinositol biosynthesis defect 4	PIG-A	37020	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060713	autosomal recessive congenital ichthyosis 4B Aliases: ARCI4B harlequin ichthyosis harlequin type ichthyosis congenita harlequin type ichthyosis fetalis	PIG-A	37020	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110064	amelogenesis imperfecta type 1H Aliases: AI1H amelogenesis imperfecta type IH	ITGB6	3694	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060479	Shwachman-Diamond syndrome Aliases: Shwachman syndrome Shwachman-Bodian-Diamond syndrome Shwachman-Diamond type metaphyseal dysplasia pancreatic insufficiency and bone marrow dysfunction	EFL1 EIF6 RPL3 SERPINI2 SRP54	3692 5276 6122 6729 79631	Homo sapiens (human)	Alliance of Genome Resources
DOID:438	autoimmune disease of the nervous system	aldoca aldocb	369193 792692	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:5154	borna disease Aliases: Enzootic encephalomyelitis	aldoca aldocb ngfb parp1	369193 560788 58133 792692	Danio rerio (zebrafish)	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	369017	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type Aliases: EBS-gen sev EBSDM epidermolysis bullosa herpetiformis Dowling-Meara type epidermolysis bullosa simplex, herpetiformis generalized severe epidermolysis bullosa simplex	Krt5	369017	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4644	epidermolysis bullosa simplex	Cd151 Krt5 Mmp9	369017 64315 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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