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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 **5251 - 5275** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:7235	pancreatic mucinous cystadenoma Aliases: pancreatic mucinous cystic neoplasm	KRAS	3845	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080322	polycystic kidney disease	ROT2	852530	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1687	neovascular glaucoma Aliases: secondary angle-closure glaucoma with rubeosis	EDN1 IL6 VEGFA	1906 3569 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050573	2-hydroxyglutaric aciduria	L2HGDH	79944	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080356	IgG4-related disease	LAT	27040	Homo sapiens (human)	Alliance of Genome Resources
DOID:813	septic arthritis Aliases: infectious arthritis	Cd4	12504	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:540	strabismus	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080998	acute necrotizing pancreatitis	Atg6 Spn28Dc TkR99D Tl chp	34091 42850 43222 43551 43690	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110637	muscular dystrophy-dystroglycanopathy type B6 Aliases: MDC1D MDDGB6 congenital muscular dystrophy LARGE-related congenital muscular dystrophy type 1D muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6 muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6	lge-1	187206	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13166	allergic bronchopulmonary aspergillosis Aliases: pulmonary aspergillus disease	cftr	559080	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:3762	cytochrome-c oxidase deficiency disease Aliases: MITOCHONDRIAL COMPLEX IV DEFICIENCY	COX1 Cox5a Cox6c	252934 26195 54322	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112233	lissencephaly 8 Aliases: LIS8	TMTC3	160418	Homo sapiens (human)	Alliance of Genome Resources
DOID:8549	chronic ulcer of skin Aliases: Callous ulcer Indolent ulcer	Icam1 Mmp9 Pdgfa Pdgfra	15894 17395 18590 18595	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112381	muscular dystrophy-dystroglycanopathy type C12 Aliases: LGMD due to POMK deficiency Limb-girdle muscular dystrophy due to POMK deficiency MDDGC12 muscular dystrophy-dystroglycanopathy, limb-girdle, POMK-related	Pomk	74653	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111933	phosphoglycerate kinase 1 deficiency Aliases: GSD due to phosphoglycerate kinase 1 deficiency PGK1 deficiency glycogen storage disease due to phosphoglycerate kinase 1 deficiency glycogenosis due to phosphoglycerate kinase 1 deficiency	PGK1	850370	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	c1galt1c1	324052	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0111258	pentosuria Aliases: L-xylulose reductase deficiency L-xylulosuria PNTSU essential pentosuria xylitol dehydrogenase deficiency	Dcxr	171408	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10588	adrenoleukodystrophy Aliases: ALD Bronze Schilder disease Encephalitis periaxialis concentrica Encephalitis periaxialis, Schilder's Siemerling-Creutzfeldt Disease X-linked adrenoleukodystrophy diffuse sclerosis sudanophilic cerebral sclerosis	W01F3.2 cri-2 zmp-3 zmp-4	178748 179197 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050954	spinocerebellar ataxia type 1	Atxn1	20238	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:687	hepatoblastoma	Cdh1 Ctnnb1 Dpep1 Fas Gpc3 Smo	246097 25236 25273 83502 84353 94199	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8634	prostate carcinoma in situ Aliases: PIN III carcinoma in situ of prostate grade III PIN	fzd4.S	399192	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0040094	autoimmune glomerulonephritis	FGL2	10875	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112373	autosomal dominant auditory neuropathy 3 Aliases: AUNA3	TMEM43	79188	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060643	primary sclerosing cholangitis	cftr vegfaa	30682 559080	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0112002	immunodeficiency 47 Aliases: CDG IIs CDG2S CDGIIs IMD47 congenital disorder of glycosylation type IIs immunodeficiency and hepatopathy with or without neurologic features	VhaAC45	35944	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources

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