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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 **5051 - 5075** of **5716** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:4074	pancreatic adenocarcinoma Aliases: pancreas adenocarcinoma	CXCR4 E2F1 JAK1 MAP2K1 MAPK9 RAC1 RAF1	1869 3716 5601 5604 5879 5894 7852	Homo sapiens (human)	Alliance of Genome Resources
DOID:4079	heart valve disease Aliases: Valvular heart disease	Galnt1 Tnf	14423 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4079	heart valve disease Aliases: Valvular heart disease	ACE COL1A2	1278 1636	Homo sapiens (human)	Alliance of Genome Resources
DOID:4079	heart valve disease Aliases: Valvular heart disease	Htr2b	29581	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	ALDH2 CPOX CYP2E1 HFE MBL2 PRKCSH SERPINA1 THBD TNF	1371 1571 217 3077 4153 5265 5589 7056 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:4154	dentinogenesis imperfecta	Dspp	666279	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4154	dentinogenesis imperfecta	COL1A1 DSPP	1277 1834	Homo sapiens (human)	Alliance of Genome Resources
DOID:4159	skin cancer Aliases: CA - skin cancer malignant neoplasm of skin melanoma and Non-melanoma skin cancer	Snai1	20613	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4166	syphilis Aliases: syphilitic chancre	KIR3DS1	3813	Homo sapiens (human)	Alliance of Genome Resources
DOID:417	autoimmune disease Aliases: autoimmune hypersensitivity disease hypersensitivity reaction type II disease	Cd200 Gpr132	17470 56696	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:417	autoimmune disease Aliases: autoimmune hypersensitivity disease hypersensitivity reaction type II disease	HLA-DQA1 HLA-DQB1 HLA-DRB1 IDH1 NOD2 PARP1 SIAE	142 3117 3119 3123 3417 54414 64127	Homo sapiens (human)	Alliance of Genome Resources
DOID:418	systemic scleroderma Aliases: Scleroderma Scleroderma syndrome progressive systemic sclerosis systemic sclerosis	Col3a1 Fbn1 Fosl2 Tgfbr1	12825 14118 14284 21812	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:418	systemic scleroderma Aliases: Scleroderma Scleroderma syndrome progressive systemic sclerosis systemic sclerosis	ANXA5 CD86 ELN ESR1 FBN1 HGF HLA-DQA1 IFNG IL1R1 IL23R LTA MMP3 MMP9 NAT2 NOTCH4 SLC11A1 STAT4	10 149233 2006 2099 2200 308 3082 3117 3458 3554 4049 4314 4318 4855 6556 6775 942	Homo sapiens (human)	Alliance of Genome Resources
DOID:4183	pseudopseudohypoparathyroidism Aliases: Normocalcemic pseudohypoparathyroidism PPHP	Gnas	14683	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4183	pseudopseudohypoparathyroidism Aliases: Normocalcemic pseudohypoparathyroidism PPHP	GNAS	2778	Homo sapiens (human)	Alliance of Genome Resources
DOID:4184	pseudohypoparathyroidism Aliases: PHP	Gnas	14683	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4184	pseudohypoparathyroidism Aliases: PHP	GNAS	2778	Homo sapiens (human)	Alliance of Genome Resources
DOID:4186	articulation disorder Aliases: Articulation impairment Phonological disorder	CNTNAP2 FOXP2	26047 93986	Homo sapiens (human)	Alliance of Genome Resources
DOID:4189	mutism	CNTNAP2	26047	Homo sapiens (human)	Alliance of Genome Resources
DOID:419	scleroderma Aliases: dermatosclerosis	HLA-A	3105	Homo sapiens (human)	Alliance of Genome Resources
DOID:4194	glucose metabolism disease Aliases: disorder of glucose metabolism	InR Tl	42549 43222	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4195	hyperglycemia	GLK1	850317	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:4195	hyperglycemia	CCL11 CYP2C9 GPX1 HP IL6 PDX1 PON1 SOD1 TF	1559 2876 3240 3569 3651 5444 6356 6647 7018	Homo sapiens (human)	Alliance of Genome Resources
DOID:4195	hyperglycemia	Avp Glp1r Hrh3 Htr2a Lepr Pcsk1 Ppargc1a Prkcb Prkcz Prnp	24221 24536 24686 25023 25051 25204 25522 29595 83516 85268	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:422	congenital structural myopathy	MTM1	4534	Homo sapiens (human)	Alliance of Genome Resources

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