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 **15126 - 15150** of **15957** in total

« First

‹ Prev

…

602

603

604

605

606

607

608

609

610

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:0110354	retinitis pigmentosa 19 Aliases: RP19	abt-2	171782	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111035	CADASIL 1 Aliases: autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1	glp-1 lin-12	176282 176286	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5517	stomach carcinoma Aliases: cancer of the stomach carcinoma of stomach gastric carcinoma	W01F3.2 let-23 ost-1 parp-1 plr-1 zmp-2 zmp-3 zmp-4	174462 175383 176575 176931 178748 179991 180351 266823	Caenorhabditis elegans	Alliance of Genome Resources
DOID:5520	head and neck squamous cell carcinoma Aliases: carcinoma of the head and neck squamous cell carcinoma of the head and neck squamous cell carcinomas of head and neck	ddr-2 let-23 srp-3	174462 178672 180622	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2378	relapsing-remitting multiple sclerosis Aliases: RRMS Relapsing-remitting MS	W01F3.2 cri-2 scav-2 scav-3 srp-3 zmp-3 zmp-4	176673 176787 178672 178748 179197 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050557	congenital muscular dystrophy	R193.2	182256	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9974	drug dependence	ace-1 ace-3 ncam-1 pgp-1 pgp-3	175076 178215 180418 181326 181706	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060717	autosomal recessive congenital ichthyosis 8 Aliases: ARCI8 lamellar ichthyosis 4 late-onset lamellar ichthyosis	lipl-1 lipl-2 lipl-3 lipl-4 lipl-5	178563 178572 179046 179771 185840	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2739	Gilbert syndrome Aliases: Constitutional hyperbilirubinemia Gilbert's disease Gilbert's syndrome Gilbert-Meulengracht syndrome hereditary nonhemolytic jaundice	ugt-61	185500	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10772	thrombotic thrombocytopenic purpura Aliases: Moschcowitz's syndrome	scav-2 scav-3	176673 176787	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13812	adhesions of uterus Aliases: Band of uterus Intrauterine adhesions Intrauterine synechiae	ver-1 ver-4	175182 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13714	anodontia Aliases: Complete absence of teeth Developmental absence of tooth Total anodontia of permanent and deciduous teeth	W01F3.2 zmp-3 zmp-4	178748 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110969	brachydactyly type B1 Aliases: BDB1	cam-1	174473	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110721	neuronal ceroid lipofuscinosis 1 Aliases: CLN1 neuronal ceroid lipofuscinosis 1 variable age of onset	ppt-1	191744	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060475	myoclonic-atonic epilepsy Aliases: EEOC childhood onset epileptic encephalopathy	snf-11	191770	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13976	peptic esophagitis Aliases: Peptic reflux disease Reflux oesophagitis reflux esophagitis	dbl-1 let-23	174462 179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	bli-3 gspd-1	171608 178046	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3744	cervical squamous cell carcinoma Aliases: squamous cell carcinoma of cervix squamous cell carcinoma of the Cervix Uteri	cri-2 timp-1 ver-4	179197 179199 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111199	autosomal dominant distal hereditary motor neuronopathy 7 Aliases: DHMN7A DHMNVPy HMN VIIA HMN7A Harper-Young myopath dHMN7 distal hereditary motor neuronopathy type 7 distal hereditary motor neuropathy type VIIA distal spinal muscular atrophy with vocal cord paralysis distal spinal muscular atrophy with vocal cord paralysis type 7A	cho-1	178274	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110034	X-linked Alport syndrome Aliases: nephropathy and deafness, X-linked	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
DOID:898	autosomal dominant polycystic kidney disease Aliases: ADPKD Congenital biliary ectasias POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1	C49C8.5 W01F3.2 Y43C5A.2 pat-2 pkd-2 zmp-3 zmp-4	176240 177668 177911 178424 178748 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060218	CREST syndrome	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14365	systemic primary carnitine deficiency disease Aliases: carnitine transporter deficiency carnitine uptake defect deficiency of plasma-membrane carnitine transporter primary carnitine deficiency renal carnitine transport defect	45566	172841	Caenorhabditis elegans	Alliance of Genome Resources
DOID:437	myasthenia gravis	ace-1 ace-3 gar-3	175076 179962 181706	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1270	hereditary hemorrhagic telangiectasia Aliases: Osler hemorrhagic telangiectasia syndrome Osler-Weber-Rendu disease Rendu-Osler-Weber disease	daf-1 sma-6	174044 176829	Caenorhabditis elegans	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