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 **5176 - 5200** of **15957** in total

« First

‹ Prev

…

204

205

206

207

208

209

210

211

212

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:480	movement disease	DRD2 EFNB3	1813 1949	Homo sapiens (human)	Alliance of Genome Resources
DOID:5425	ovarian hyperstimulation syndrome Aliases: secondary Meig's syndrome	DRD2 F3 FSHR IL6 KDR NR1H3 SERPINF1 TFPI VEGFA	10062 1813 2152 2492 3569 3791 5176 7035 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:251	alcohol-induced mental disorder	DRD2 FOXO4	1813 4303	Homo sapiens (human)	Alliance of Genome Resources
DOID:1742	drug psychosis Aliases: Drug-induced psychosis Drug-induced psychotic disorder	DRD2 GAD1 GAD2 OPRM1	1813 2571 2572 4988	Homo sapiens (human)	Alliance of Genome Resources
DOID:4990	essential tremor Aliases: benign essential tremor essential hereditary tremor shaky hand syndrome	DRD3 MAPT	1814 4137	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050425	restless legs syndrome Aliases: WED Willis-Ekbom disease Wittmaack-Ekbom syndrome	DRD3 MEIS1 PTPRD SLC11A2 TF	1814 4211 4891 5789 7018	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111428	essential tremor 1 Aliases: ETM1 hereditary essential tremor 1	DRD3	1814	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060040	pervasive developmental disorder Aliases: Pervasive Child Development Disorders pervasive development disorder	DRD4 DRD5	1815 1816	Homo sapiens (human)	Alliance of Genome Resources
DOID:529	blepharospasm	DRD5	1816	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110082	arrhythmogenic right ventricular dysplasia 11 Aliases: ARVC11 ARVD11 arrhythmogenic right ventricular cardiomyopathy 11 familial arrhythmogenic right ventricular dysplasia 11	DSC2	1824	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080737	Ehlers-Danlos syndrome musculocontractural type 2	DSE	29940	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081108	keratosis palmoplantaris striata 1	DSG1	1828	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110081	arrhythmogenic right ventricular dysplasia 10 Aliases: ARVC10 ARVD10 arrhythmogenic right ventricular cardiomyopathy 10 familial arrhythmogenic right ventricular dysplasia 10	DSG2	1829	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110458	dilated cardiomyopathy 1BB Aliases: CMD1BB	DSG2	1829	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060851	pemphigus vulgaris Aliases: familial pemphigus vulgaris	DSG3 HLA-DQB1	1830 3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110703	hypotrichosis 6 Aliases: Hypotrichosis, Localized, Autosomal Recessive 1 Hypt6 Lah1 Monilethrix-like hypotrichosis autosomal recessive localized hypotrichosis	DSG4	147409	Homo sapiens (human)	Alliance of Genome Resources
DOID:4535	hypotrichosis	DSG4	147409	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110076	arrhythmogenic right ventricular dysplasia 8 Aliases: ARVC8 ARVD8 arrhythmogenic right ventricular cardiomyopathy 8 familial arrhythmogenic right ventricular dysplasia 8	DSP	1832	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081109	keratosis palmoplantaris striata 2	DSP	1832	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090128	Carvajal syndrome Aliases: DCWHK dilated cardiomyopathy with woolly hair and keratoderma palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair	DSP	1832	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070151	hereditary sensory and autonomic neuropathy type 6 Aliases: HSAN6 hereditary sensory and autonomic neuropathy type VI	DST	667	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110774	hereditary spastic paraplegia 23 Aliases: Lison syndrome SPG23 Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome spastic paraplegia 23 spastic paraplegia with pigmentary abnormalities	DSTYK	25778	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080206	CAKUT1 Aliases: Congenital anomalies of the kidney and urinary tract 1	DSTYK	25778	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060545	Hermansky-Pudlak syndrome 7	DTNBP1	84062	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050338	primary bacterial infectious disease	DUOX1 DUOX2 GLI1 GLI2 GLI3 IHH SHH SMO	2735 2736 2737 3549 50506 53905 6469 6608	Homo sapiens (human)	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