GlyCosmos Portal

GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Database	Last Updated
Alliance of Genome Resources	February 28, 2024
DisGeNET	February 14, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Disease ID	Disease Name	Gene Symbol	Gene ID ▼
DOID:557	kidney disease	CDC42 CDC42 Cdc42 Cdc42 Cdc42 ELOVL5 FADS2 G6PD GBA3 KL KLB Kl Kl Klb LCT LCTL LIPC Lctl Lipc RAC1 RAC3 Rac1 Rac1 Rac3 UMOD XYLT1 Xylt1 Xylt1 oxt sqv-6 xylt1 xylt1	100145490 12540 152831 15450 16591 170758 190099 19353 197021 233781 235435 2539 32981 363875 38288 3938 3990 560951 57733 5879 5881 60481 64131 64133 64465 7369 83379 83504 850930 9365 9415 998
DOID:0060462	Desbuquois dysplasia	CANT1 Cant1 Cant1 XYLT1 Xylt1 Xylt1 apy-1 oxt sqv-6 xylt1.L xylt1.S xylt1 xylt1	100145490 108703114 124583 181019 190099 233781 246272 38288 444363 560951 64131 64133 76025
DOID:2738	pseudoxanthoma elasticum	C27A7.3 CAT ENPP1 Enpp1 Enpp1 GPX1 NPP1 NPP2 XYLT1 XYLT2 Xylt1 Xylt1 Xylt2 Xylt2 oxt sqv-6 xylt1.L xylt1.S xylt1 xylt1 xylt2.L xylt2 xylt2	100145490 108701100 108703114 179665 18605 190099 217119 233781 2876 38288 444363 448400 5167 560951 563446 64131 64132 64133 64134 847 850391 85496 856699
DOID:0110635	muscular dystrophy-dystroglycanopathy type B5	CG15651 FKRP Fkrp Fkrp fkrp.L fkrp fkrp	100145309 108698503 243853 308390 37375 571426 79147
DOID:0111241	congenital muscular dystrophy-dystroglycanopathy type A5	CG15651 FKRP Fkrp Fkrp fkrp.L fkrp fkrp	100145309 108698503 243853 308390 37375 571426 79147
DOID:11724	limb-girdle muscular dystrophy	CG15651 FKRP Fkrp Fkrp KL fkrp.L fkrp fkrp	100145309 108698503 243853 308390 37375 571426 79147 9365
DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I	CG15651 FKRP Fkrp Fkrp KL fkrp.L fkrp fkrp	100145309 108698503 243853 308390 37375 571426 79147 9365
DOID:12930	dilated cardiomyopathy	ACE ACT1 ACTC1 Actc1 Actc1 CAT CG15651 CG1598 CS CYP1A1 CYP2C19 DAG1 DNM1 DNM1L Dg Dnm1l Dnm1l EEF1A1 Eef1a1 Eef1a1 FADS2 FKRP FOL2 Fkrp Fkrp GCH1 GET3 GET3 GPX1 Gch1 Gch1 Get3 Get3 ICAM1 PDE2 PDE9A PPA2 Pde9 Pde9a Pde9a Pu actc1.L actc1 asna-1 cat-4 dnm1l drp-1 eef1a1l1 fkrp.L fkrp fkrp get3.S get3 get3 ttn.2	100145309 10059 101669768 108698503 114114 11464 13627 1431 14528 1543 1557 1605 1636 171361 176254 177336 179472 18585 1915 191569 243853 2643 2876 288919 29244 29275 30516 308390 32233 325704 3383 35690 36773 37375 37415 379752 393896 394698 439 444297 5152 56495 571426 70 74006 779794 79147 847 850504 850686 851458 853183 854542 855309 9415
DOID:0110777	hereditary spastic paraplegia 26	B4GALNT1 B4galnt1 B4galnt1 b4galnt1.L b4galnt1.S b4galnt1 b4galnt1a b4galnt1b	100145208 108709867 14421 2583 379299 558684 64828 793635
DOID:0080738	Ehlers-Danlos syndrome spondylodysplastic type 1	B4GALT7 B4galt7 B4galt7 b4galt7.L b4galt7.S b4galt7 b4galt7 sqv-3 ﾎｲ4GalT7	100144979 108710989 11285 176382 218271 364675 42991 445022 495369