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 **6226 - 6250** of **15957** in total

« First

‹ Prev

…

246

247

248

249

250

251

252

253

254

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:0111162	epidermal nevus Aliases: nonepidermolytic keratinocytic nevus	Pik3ca	18706	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6498	seborrheic keratosis	Pik3ca	18706	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081001	Cowden syndrome 5	Pik3ca	18706	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:7305	astroblastoma	Pik3r1	18708	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111949	immunodeficiency 36 Aliases: IMD36 activated phosphoinositide 3-kinase delta syndrome 2	Pik3r1	18708	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111454	SHORT syndrome Aliases: Aarskog-Ose-Pande syndrome Lipodystrophy-Rieger anomaly-diabetes syndrome Rieger anomaly-partial lipodystrophy syndrome short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay	Pik3r1	18708	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081139	agammaglobulinemia 7	Pik3r1	18708	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060653	lethal congenital contracture syndrome 3 Aliases: Israeli Bedouin type B multiple contracture syndrome	Pip5k1c	18717	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111242	congenital muscular dystrophy-dystroglycanopathy type A6 Aliases: MDDGA6 Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6	lge-1	187206	Caenorhabditis elegans	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:1508	candidiasis Aliases: Disseminated candidiasis systemic candidiasis	fut-4 fut-5 fut-6	187342 188084 3565968	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110658	congenital myasthenic syndrome 15 Aliases: CMS15 congenital myasthenic syndrome 15 without tubular aggregates	algn-14	187398	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050964	spinocerebellar ataxia type 14	Prkcg	18752	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110859	polycystic kidney disease 2 Aliases: Apkd2 Pkd2 Polycystic Kidney Disease, Adult, Type II	Pkd2 Pkd2l1 Pkd2l2	18764 329064 53871	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080411	familial adenomatous polyposis 3	nth-1	187770	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2615	papilloma Aliases: papillomatosis	Pla2g4a	18783	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1247	blood coagulation disease Aliases: coagulation protein disease postpartum coagulation defect postpartum coagulation defect with delivery	Plat	18791	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14566	disease of cellular proliferation Aliases: cell process disease neoplasm	Plaur Spp1 Tfpi Trp53	18793 20750 21788 22059	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11729	Lyme disease Aliases: Bannwarth syndrome Bannworth's syndrome Lyme borreliosis Neurological Lyme disease lyme neuroborreliosis neuroborreliosis	Plaur	18793	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112303	spondylometaphyseal dysplasia with corneal dystrophy Aliases: SMDCD	Plcb3	18797	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080081	nonsyndromic congenital nail disorder 3	Plcd1	18799	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080288	spinocerebellar ataxia 46	Pld3	18807	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110160	Charcot-Marie-Tooth disease axonal type 2T Aliases: AR-CMT2T CMT2T Charcot-Marie-Tooth neuropathy type 2T autosomal recessive axonal Charcot-Marie-Tooth disease type 2T	nep-2	188090	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111745	cerebellar ataxia type 43 Aliases: SCA43	nep-2	188090	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy Aliases: epidermolysis bullosa simplex and limb-girdle muscular dystrophy limb-girdle muscular dystrophy with epidermolysis bullosa simplex	Plec	18810	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