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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 **9326 - 9350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0050802	Ehlers-Danlos syndrome spondylodysplastic type 2 Aliases: EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 Ehlers-Danlos syndrome progeroid type	sqv-2	173635	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4249	Gerstmann-Straussler-Scheinker syndrome Aliases: Gerstmann-Straussler-Scheinker disease PRION DEMENTIA	PRNP	5621	Homo sapiens (human)	Alliance of Genome Resources
DOID:9975	cocaine dependence	BDNF CAMK4 CCSER1 CHRNA3 CHRNB3 COL21A1 COMT CREB1 DRD2 EGR1 FOS FOSB GABBR1 GRIA1 HTR2A HTR2C HTR3A MANEA NGF OPRD1 OPRK1 OPRM1 PER2 PRL SIRT1 SIRT2 TENM3	1136 1142 1312 1385 1813 1958 22933 23411 2353 2354 2550 2890 3356 3358 3359 401145 4803 4985 4986 4988 55714 5617 627 79694 814 81578 8864	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080199	colorectal carcinoma	Axn Idgf1 Idgf2 Idgf3 Idgf4 Idgf5 Idgf6 Ptp10D mys	31926 32115 34978 34979 34981 36868 37104 43565 44885	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050861	colorectal adenocarcinoma	Abcb1a Abcb1b Braf Brd8 Car12 Cd44 Erbb3 Ezh2 Fam151a Fgfr2 Flt3 Fos Gpx4 Gsk3b Il16 Jun Kcnh1 Kdr Kmt2b Ncoa2 Pcsk4 Rnaset2a Rnaset2b Slc7a5 Stat5b Stra6 Tpst1 Trp53	100037283 109880 12505 13867 14056 14183 14255 14281 16170 16476 16510 16542 17978 18551 18669 18671 20539 20851 20897 22021 22059 230579 56637 625249 68195 75410 76459 78656	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:824	periodontitis Aliases: chronic pericementitis	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:14557	primary pulmonary hypertension Aliases: Idiopathic pulmonary arterial hypertension	Adora2a Fgfr2 Kcnk3 Pparg Tnfsf4 Vip	117064 25022 25369 25664 29553 89814	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2615	papilloma Aliases: papillomatosis	Pla2g4a	18783	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110444	dilated cardiomyopathy 1X Aliases: CMD1X dilated cardiomyopathy with mild or no proximal muscle weakness	Fktn	246179	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12986	leukostasis	Ace Serpinf1	11421 20317	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10908	hydrocephalus Aliases: hydrocephalus, X-linked hydrocephalus, nonsyndromic, autosomal recessive	ntf3.L	399298	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0112072	nuclear type mitochondrial complex I deficiency 20 Aliases: ACAD9 deficiency Acyl-CoA dehydrogenase 9 deficiency MC1DN20 mitochondrial complex 1 deficiency due to ACAD9 deficiency	Acad9	229211	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110225	Brugada syndrome 8 Aliases: BRGDA8	HCN4	10021	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081210	autosomal recessive intellectual developmental disorder 46	hst-1	177675	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11714	gestational diabetes Aliases: GDM Gestational diabetes mellitus Maternal gestational diabetes mellitus	ECM38 EMI2 GLK1 HXK1 HXK2 OGG1	850317 850614 851006 852128 852639 854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111517	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Aliases: PEOA2 autosomal dominant progressive external ophthalmoplegia 2	Slc25a4 Slc25a5	11739 11740	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070219	familial hyperinsulinemic hypoglycemia 1 Aliases: HHF1	ABCC8	6833	Homo sapiens (human)	Alliance of Genome Resources
DOID:2772	irritant dermatitis Aliases: irritant contact dermatitis primary irritant dermatitis	IL4	3565	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111100	maturity-onset diabetes of the young type 2 Aliases: MODY glucokinase-related MODY type 2 MODY2	GCK	2645	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080137	multiple endocrine neoplasia type 4 Aliases: Multiple Endocrine Neoplasia, Type IV	CDKN1B	1027	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050577	cranioectodermal dysplasia Aliases: Levin syndrome Sensenbrenner syndrome	SEC12	855760	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050883	infantile cerebellar-retinal degeneration	Aco2	79250	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080006	bone development disease	Csf1r Flnb Lrp4 Npr2 Tnfrsf11a	12978 21934 228357 230103 286940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110658	congenital myasthenic syndrome 15 Aliases: CMS15 congenital myasthenic syndrome 15 without tubular aggregates	ALG14	199857	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080946	retinal dystrophy with leukodystrophy Aliases: ACBD5 deficiency	ACBD5	91452	Homo sapiens (human)	Alliance of Genome Resources

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