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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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **5326 - 5350** of **5716** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:6432	pulmonary hypertension	ACE2 ACVRL1 ADM AGTR1 ALOX5 ATP2A2 BMPR2 CSF3 CYP2J2 EDNRA EPAS1 EPO F5 HP IL1RN IL23R MMP9 NOS2 NOS3 PTGIS PTK2 SERPINE1 SLC6A4 TGFB1 VEGFB VWF	133 1440 149233 1573 185 1909 2034 2056 2153 240 3240 3557 4318 4843 4846 488 5054 5740 5747 59272 6532 659 7040 7423 7450 94	Homo sapiens (human)	Alliance of Genome Resources
DOID:6432	pulmonary hypertension	Cavin1	19285	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6432	pulmonary hypertension	Agt Atp5f1a Atp5pf Bdkrb2 Cxcr4 Cysltr1 Ednra Ednrb Esr2 Fgfr1 Hmgb1 Hmgcr Kcnk3 Mmp9 Myc Nos3 Nox1 Pecam1 Ptgs2 Serpina1 Serpine1 Slc6a4 Tacr1 Tacr2 Tgfbr1 Tnc Vip	114099 114243 116640 117064 24179 24326 24577 24600 24617 24648 24807 25007 25149 25245 25459 25553 25675 29527 29553 29583 29591 50672 60628 65262 79114 81687 94271	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:648	kuru Aliases: kuru encephalopathy	PRNP	5621	Homo sapiens (human)	Alliance of Genome Resources
DOID:649	prion disease Aliases: Prion disease pathway Prion protein disease Spongiform Encephalopathy prion induced disorder transmissible spongiform encephalopathy	SOD1	6647	Homo sapiens (human)	Alliance of Genome Resources
DOID:6498	seborrheic keratosis	PIK3CA	5290	Homo sapiens (human)	Alliance of Genome Resources
DOID:65	connective tissue disease Aliases: connective tissue disorder disorder of connective tissue	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:65	connective tissue disease Aliases: connective tissue disorder disorder of connective tissue	SNRPA1 SNRPA SNRPB2 SNRPC SNRPD1	6626 6627 6629 6631 6632	Homo sapiens (human)	Alliance of Genome Resources
DOID:653	purine-pyrimidine metabolic disorder Aliases: inborn errors of purine-pyrimidine metabolism	ATIC PNP UMPS	471 4860 7372	Homo sapiens (human)	Alliance of Genome Resources
DOID:6543	acne Aliases: Acne varioliformis acne vulgaris frontalis acne	IL4R TLR2 TNF TNFRSF1A TNFRSF1B	3566 7097 7124 7132 7133	Homo sapiens (human)	Alliance of Genome Resources
DOID:655	inherited metabolic disorder Aliases: Inborn Errors of Metabolism Metabolic hereditary disorder inborn metabolism disorder	BCHE GPHN HSD11B2 LIG1 MMAB NDUFS1 NDUFS2 SLC22A5 SLC25A19	10243 326625 3291 3978 4719 4720 590 60386 6584	Homo sapiens (human)	Alliance of Genome Resources
DOID:657	adenoma Aliases: acinar cell adenoma acinic cell adenoma adenomas	APC	324	Homo sapiens (human)	Alliance of Genome Resources
DOID:6612	leukocyte adhesion deficiency Aliases: Congenital leukocyte adherence deficiency	ITGB2	3689	Homo sapiens (human)	Alliance of Genome Resources
DOID:6652	diffuse idiopathic skeletal hyperostosis Aliases: Ankylosing vertebral hyperostosis DISH Disseminated idiopathic skeletal hyperostosis	Slc29a1	63959	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6688	autoimmune lymphoproliferative syndrome Aliases: ALPS Canale-Smith syndrome	Fas Fasl	14102 14103	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6688	autoimmune lymphoproliferative syndrome Aliases: ALPS Canale-Smith syndrome	FAS FASLG	355 356	Homo sapiens (human)	Alliance of Genome Resources
DOID:670	amphetamine abuse	AKT1 COMT GABBR1 GABRG2 GAD1 GAD2 NPY1R	1312 207 2550 2566 2571 2572 4886	Homo sapiens (human)	Alliance of Genome Resources
DOID:670	amphetamine abuse	Snca	29219	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:670	amphetamine abuse	cat-1	180837	Caenorhabditis elegans	Alliance of Genome Resources
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	AGT AGTR1 APOE G6PD GLCE LMNA NR1H3 P2RY12 SELE	10062 183 185 2539 26035 348 4000 6401 64805	Homo sapiens (human)	Alliance of Genome Resources
DOID:674	cleft palate Aliases: Palatoschisis	Specc1l	74392	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:674	cleft palate Aliases: Palatoschisis	COL11A2 COL2A1 FLNB GDF6 MTHFD1 NECTIN1 ROR2 SDC2	1280 1302 2317 392255 4522 4920 5818 6383	Homo sapiens (human)	Alliance of Genome Resources
DOID:676	juvenile rheumatoid arthritis Aliases: Pauciarticular onset juvenile chronic arthritis Still's disease acute juvenile rheumatoid arthritis juvenile chronic polyarthritis juvenile idiopathic arthritis monarticular juvenile rheumatoid arthritis pauciarticular juvenile arthritis systemic juvenile rheumatoid arthritis	CCR5 CIITA HFE HLA-DQA1 HLA-DQB1 HLA-DRB1 IL1A LACC1 SLC11A1 SLC26A2	1234 144811 1836 3077 3117 3119 3123 3552 4261 6556	Homo sapiens (human)	Alliance of Genome Resources
DOID:678	progressive supranuclear palsy Aliases: Steele-Richardson-Olszewski syndrome progressive supranuclear ophthalmoplegia	MAP2K6 MAPT NAT2	10 4137 5608	Homo sapiens (human)	Alliance of Genome Resources
DOID:680	tauopathy	MAPT	4137	Homo sapiens (human)	Alliance of Genome Resources

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