GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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 **12001 - 12025** of **15957** in total

« First

‹ Prev

…

477

478

479

480

481

482

483

484

485

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:980	choroidal sclerosis Aliases: Choroidal degenerations	Gucy2e Prph2	14919 19133	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050534	congenital stationary night blindness Aliases: congenital essential nyctalopia	Cacna1f Gucy2e Nyx Trpm1	14919 17364 236690 54652	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060780	congenital diarrhea 6 Aliases: chronic diarrhea due to guanylate cyclase 2C overactivity chronic diarrhoea due to guanylate cyclase 2C overactivity congenital diarrhoea 6	Gucy2c	14917	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090142	cystathioninuria Aliases: cystathionase deficiency cystathione gamma-lyase deficiency syndrome gamma-cystathionase deficiency	CTH	1491	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050749	peripheral T-cell lymphoma	IRF4 RC3H1	149041 3662	Homo sapiens (human)	Alliance of Genome Resources
DOID:57	aortic valve insufficiency Aliases: Rheumatic aortic insufficiency Rheumatic aortic regurgitation Rheumatic aortic valve regurgitation aortic incompetence aortic insufficiency aortic regurgitation rheumatic aortic valve insufficiency	CCN2 MBL2	1490 4153	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080001	bone disease	CCN2 FGFR1 FGFR2 FGFR3 FGFR4 NPR3 PON1	1490 2260 2261 2263 2264 4883 5444	Homo sapiens (human)	Alliance of Genome Resources
DOID:9477	pulmonary embolism Aliases: pulmonary artery embolism pulmonary embolus	CCL2 CCN2 CX3CL1 EDN1 F13A1 F2 F5 FGA FGB FGG FTO HP HPR MMP2 MMP9 NOS3 NPPB PROC TBXAS1 VCAM1	1490 1906 2147 2153 2162 2243 2244 2266 3240 3250 4313 4318 4846 4879 5624 6347 6376 6916 7412 79068	Homo sapiens (human)	Alliance of Genome Resources
DOID:397	restrictive cardiomyopathy Aliases: Cardiomyopathy, constrictive primary restrictive cardiomyopathy	CCN2 DES MAP2K3 MAP2K6 MYH15 MYH1 MYH7 MYPN SCD5 SCD TNNI3	1490 1674 22989 4619 4625 5606 5608 6319 7137 79966 84665	Homo sapiens (human)	Alliance of Genome Resources
DOID:12932	endomyocardial fibrosis Aliases: African endomyocardial fibrosis Becker's disease Endomyocardial sclerosis obscure African cardiomyopathy	ACE CCL2 CCN2 UTS2R	1490 1636 2837 6347	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080234	Clark-Baraitser syndrome Aliases: Baraitser syndrome CLABARS autosomal dominant intellectual disability 49 autosomal dominant mental retardation 49	Trip12	14897	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111230	congenital muscular dystrophy-dystroglycanopathy type A11 Aliases: MDDGA11 Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11	B3GALNT2	148789	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111027	hemochromatosis type 2A Aliases: HFE2A	HJV	148738	Homo sapiens (human)	Alliance of Genome Resources
DOID:2352	hemochromatosis Aliases: Haemochromatosis diabetes bronze iron storage disorder	B2M HFE HJV TFR2 TNF	148738 3077 567 7036 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081034	glutatione synthetase deficiency with 5-oxoprolinuria	Gss	14854	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112252	glutathione synthetase deficiency of erythrocytes Aliases: glutathione synthetase deficiency without 5-oxoprolinuria	Gss	14854	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080699	glutathione synthetase deficiency	Gss	14854	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11088	asphyxia neonatorum Aliases: Asphyxia - birth Asphyxia, in liveborn infant Birth asphyxia postnatal asphyxia	Map2 Pdia3	14827 17756	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions	Grn	14824	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110732	neuronal ceroid lipofuscinosis 11 Aliases: CLN11	Grn	14824	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080286	spinocerebellar ataxia 44	Grm1	14816	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080062	autosomal recessive spinocerebellar ataxia 13 Aliases: SCAR13	Grm1	14816	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10966	lipoid nephrosis Aliases: Minimal Change Glomerulonephritis Minimal change disease Nephrotic syndrome with lesion of minimal change glomerulonephritis Nephrotic syndrome with lesion of minimal change nephrotic syndrome	Il13 Il17a Nr3c1 Stat6	14815 16163 16171 20852	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8689	anorexia nervosa	Htr4 Igfals Nr3c1	14815 15562 16005	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14320	generalized anxiety disorder	Gper1 Htr1a Htr1b Htr2b Nr3c1 Slc6a4 Zfp462	14815 15550 15551 15559 15567 242466 76854	Mus musculus (house mouse)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements