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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	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4076 - 4100** of **4649** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:4079	heart valve disease Aliases: Valvular heart disease	ACE COL1A2 GALNT1 HTR2B LRP5 MMP2 MMP9 TNF	1278 1636 2589 3357 4041 4313 4318 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	ALDH2 CPOX CYP2E1 DPYD FAS FASLG GLUL HFE HLA-DPB1 KDSR KRT18 MBL2 MDM2 PRKCSH SERPINA1 THBD TNF	1371 1571 1806 217 2531 2752 3077 3115 355 356 3875 4153 4193 5265 5589 7056 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:4137	common bile duct disease	SLC25A12 SLC25A13	10165 8604	Homo sapiens (human)	Alliance of Genome Resources
DOID:4138	bile duct disease Aliases: bile duct disorder disorder of bile duct	F3	2152	Homo sapiens (human)	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	ANXA7 CRKL MRE11 SNAI1 SRSF6	1399 310 4361 6431 6615	Homo sapiens (human)	Alliance of Genome Resources
DOID:4166	syphilis Aliases: syphilitic chancre	CCR5 KIR3DS1 NEFL TREM2	1234 3813 4747 54209	Homo sapiens (human)	Alliance of Genome Resources
DOID:417	autoimmune disease Aliases: autoimmune hypersensitivity disease hypersensitivity reaction type II disease	AHNAK B2M C9orf72 CD200 GPR132 HLA-DQA1 HLA-DQB1 HLA-DRB1 IDH1 NOD2 PARP1 SIAE	142 203228 29933 3117 3119 3123 3417 4345 54414 567 64127 79026	Homo sapiens (human)	Alliance of Genome Resources
DOID:418	systemic scleroderma Aliases: Scleroderma Scleroderma syndrome progressive systemic sclerosis systemic sclerosis	ACE ADAMTS13 AGER AGT ANXA5 BDNF C3 CCL2 CCR6 CD86 CFB CHI3L1 CLU COL1A1 COL3A1 CP CSF1 CX3CL1 CXCL16 CXCR3 CXCR6 EDN1 ELN ESR1 F11R F2 FBN1 FLI1 FLT4 FOSL2 GPX3 HGF HLA-DQA1 HMGB1 ICAM1 IFNG IGFBP3 IL13 IL13RA1 IL17A IL1R1 IL23R IL27RA IL2 IL4 IL6 JAM3 KDR LTA MMP1 MMP3 MMP9 MUC1 NGF NOTCH4 PECAM1 PTGS2 RBP4 SELENOP SERPINE1 SERPINF2 SLC11A1 STAT4 TGFBR1 VEGFA VWF	10663 11093 1116 1191 1235 1277 1281 1356 1435 149233 1636 177 183 1906 2006 2099 2147 2200 2313 2324 2355 2833 2878 308 3082 3117 3146 3383 3458 3486 3554 3558 3565 3569 3596 3597 3605 3791 4049 4312 4314 4318 4582 4803 4855 5054 50848 5175 5345 5743 58191 5950 627 629 6347 6376 6414 6556 6775 7046 718 7422 7450 83700 942 9466	Homo sapiens (human)	Alliance of Genome Resources
DOID:4183	pseudopseudohypoparathyroidism Aliases: Normocalcemic pseudohypoparathyroidism	GNAS	2778	Homo sapiens (human)	Alliance of Genome Resources
DOID:4184	pseudohypoparathyroidism	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	DGKA DGKB DGKG EIF2S3 GCK HK1 HK2 HK3 HKDC1 IGF1R INSR INSRR IRS1 IRS2 IRS4 KCNH6 PIK3CB PIK3CD RPS6KB1 TLR4 TLR5	1606 1607 1608 1968 2645 3098 3099 3101 3480 3643 3645 3667 5291 5293 6198 7099 7100 80201 81033 8471 8660	Homo sapiens (human)	Alliance of Genome Resources
DOID:4195	hyperglycemia	ADRB1 AKR1B1 AVP CBL CCL11 CYP11A1 CYP2C9 DRD1 EPAS1 F2 F7 GCK GIPR GLP1R GPX1 HCRTR2 HK2 HK3 HKDC1 HP HRH3 HSPD1 HSPG2 HTR2A ICAM1 IL1A IL1RN IL6 ITGAM ITGAV LDHA LEPR MMP9 PCSK1 PDX1 PKLR PLA2G4A PON1 PPARGC1A PRNP PTCH1 SDC1 SOD1 TF TSHB	10891 11255 153 1559 1583 1812 2034 2147 2155 231 2645 2696 2740 2876 3062 3099 3101 3240 3329 3339 3356 3383 3552 3557 3569 3651 3684 3685 3939 3953 4318 5122 5313 5321 5444 551 5621 5727 6356 6382 6647 7018 7252 80201 867	Homo sapiens (human)	Alliance of Genome Resources
DOID:4202	brain stem glioma Aliases: Brainstem Neuroglial tumor	PDGFRA	5156	Homo sapiens (human)	Alliance of Genome Resources
DOID:422	congenital structural myopathy	ACTB MTM1	4534 60	Homo sapiens (human)	Alliance of Genome Resources
DOID:4226	endometrial stromal sarcoma Aliases: ESS Undifferentiated endometrial sarcoma endometrial stromal sarcoma, high grade	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:423	myopathy	ACTB CLCN2 CLCNKB COL15A1 COL18A1 COL4A1 COL4A3 COL4A4 COL4A5 COL4A6 DNM2 FHL1 FLNA FLNB FLNC HMGCR HNRNPA1 HNRNPA1L2 HNRNPA2B1 HNRNPA3 LDB3 LMNA LMNB1 LMNB2 MEGF10 MEGF11 MTM1 MTMR1 MTMR2 MYBPC2 MYH15 MYH1 MYH7 NPL PDLIM5 PDLIM7 PEAR1 PSMC5	10611 11155 1181 1188 1282 1285 1286 1287 1288 1306 144983 1785 220988 2273 22989 2316 2317 2318 3156 3178 3181 375033 4000 4001 4534 4606 4619 4625 5705 60 80781 80896 84465 84466 84823 8776 8898 9260	Homo sapiens (human)	Alliance of Genome Resources
DOID:4231	histiocytoma	KLRC4-KLRK1 KLRK1	100528032 22914	Homo sapiens (human)	Alliance of Genome Resources
DOID:4239	alveolar soft part sarcoma	ASPSCR1	79058	Homo sapiens (human)	Alliance of Genome Resources
DOID:4247	coronary restenosis	BCHE CDH13 CXCR3 ITGB2 LOX MBL2 MYC NPY5R SPP1 TNF TP53 UCP3	1012 2833 3689 4015 4153 4609 4889 590 6696 7124 7157 7352	Homo sapiens (human)	Alliance of Genome Resources
DOID:4248	coronary stenosis Aliases: Coronary artery stenosis	CYP2R1 EDN1 IGF1R ITGAV MDK PECAM1 TNFRSF11B	120227 1906 3480 3685 4192 4982 5175	Homo sapiens (human)	Alliance of Genome Resources
DOID:4249	Gerstmann-Straussler-Scheinker syndrome Aliases: Gerstmann-Straussler-Scheinker disease PRION DEMENTIA	PRNP	5621	Homo sapiens (human)	Alliance of Genome Resources

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