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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 **15076 - 15100** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0080158	herpes simplex virus keratitis Aliases: dendritic keratitis	APOE IL1RN TLR4	348 3557 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110014	age related macular degeneration 1 Aliases: ARMD1 age related maculopathy 1	APOE CFHR1 CFHR3 HMCN1 VLDLR	10878 3078 348 7436 83872	Homo sapiens (human)	Alliance of Genome Resources
DOID:10211	cholelithiasis	APOE CCKAR CFTR CYP17A1 UGT1A1	1080 1586 348 54658 886	Homo sapiens (human)	Alliance of Genome Resources
DOID:13550	angle-closure glaucoma Aliases: ACG - Angle-closure glaucoma Angle Closure Glaucoma Closed angle glaucoma Narrow cleft glaucoma primary open-angle glaucoma with narrow angles	APOE CAT EDN1 HGF LOXL1 MMP9 MUC5AC NOS3 TFAP2B	1906 3082 348 4016 4318 4586 4846 7021 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:12894	Sjogren's syndrome Aliases: Sicca syndrome Sjogren syndrome xerodermosteosis	APOE BDNF BST2 CAST CCR5 CCR7 CD40LG CTLA4 CYP19A1 CYP1A1 E2F1 FAS GDNF HLA-DQA1 HLA-DQB1 HLA-DRB1 HNRNPH1 ICAM1 IFNG IL10 IL13 IL1RN IL23R IL2 IL2RA IL4 IL6 LTA MMP3 MMP9 MUC16 MUC19 MUC5AC NEFL PON1 REG1A SATB1 SELP ST14 STAT4 TGFB1 THBS1 TNF TNFSF13B TRAF3IP2 VIM	10673 10758 1234 1236 149233 1493 1543 1588 1869 2668 283463 3117 3119 3123 3187 3383 3458 348 355 3557 3558 3559 3565 3569 3586 3596 4049 4314 4318 4586 4747 5444 5967 627 6304 6403 6768 6775 684 7040 7057 7124 7431 831 94025 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:10003	sensorineural hearing loss Aliases: High Frequency Hearing Loss High frequency deafness Perceptive deafness Perceptive hearing loss Perceptive hearing loss or deafness Sensorineural Deafness Sensory hearing loss central hearing loss high-frequency hearing loss	APOE ATP1A1 ATP1B1 CAT DIAPH1 DNAAF4 DNAH17 DNAH9 EDNRB EYA4 F2 F5 GATA3 HLA-B HLA-DRB1 IFNG IL2 ITGA2 MBL2 MYH14 MYH9 MYO15A MYO1A MYO6 MYO7A NGF PSMC3 PTGDS SCARB1 SLC12A2 SLC44A4 SLC7A14 SLITRK6 SOD2 STRC TECTA TMPRSS3 TNF WFS1 WHRN	161497 161582 1729 1770 1910 2070 2147 2153 25861 2625 3106 3123 3458 348 3558 3673 4153 4627 4640 4646 4647 476 4803 481 51168 5702 5730 57709 64699 6558 6648 7007 7124 7466 79784 80736 84189 847 8632 949	Homo sapiens (human)	Alliance of Genome Resources
DOID:5679	retinal disease	APOE AQP4 CAT CEPT1 CHPT1 GFAP GRK1 IL10 MAP2K3 PISD PLCB4 PRPH2 THY1	10390 23761 2670 348 3586 361 5332 5606 56994 5961 6011 7070 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:332	amyotrophic lateral sclerosis Aliases: ALS Lou Gehrig's disease motor neuron disease, bulbar	APOE AQP4 ATP13A2 ATP13A3 ATP13A5 BPTF C3 C5AR1 C9orf72 CASP9 CCR2 CHMP2B DCTN1 DPP6 EIF2AK2 EPG5 EPO EWSR1 FUS GDNF GOT1 GRN GSK3A GSK3B HDAC4 HMGB1 IGF1R IGF2R ITIH4 ITPR2 KDR KEAP1 KIF1B LCN2 LRRK2 MAP4 MAPT MMP1 MMP2 MMP9 MSTN NEFH NEFL NEFM NFE2L2 NRG1 OPTN PGF PON2 PON3 PPARGC1A PSMC4 PSMC5 PTGS2 PTPRZ1 SARM1 SERPINF1 SLC11A2 SLC1A2 SOD1 SOD3 SQSTM1 TARDBP TFAM UBQLN1 UBQLN2 UBQLN3 UBQLN4 UNC13A VAPA VAPB VEGFA ZNF106	10133 10891 120892 1639 1804 203228 2056 2130 2186 23025 23095 23098 23400 23435 2521 25978 2660 2668 2805 2896 2931 2932 29978 29979 3084 3146 344905 348 3480 3482 361 3700 3709 3791 3934 4134 4137 4312 4313 4318 4741 4744 4747 4780 4891 50613 5176 5228 5445 5446 5610 56893 5704 5705 5743 57724 5803 64397 6506 6647 6649 7019 718 728 729230 7422 79572 842 8878 9217 9218 9759 9817	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111370	apolipoprotein C-III deficiency Aliases: HALP2 hyperalphalipoproteinemia 2	APOC3	345	Homo sapiens (human)	Alliance of Genome Resources
DOID:2972	renal artery obstruction	APOC3 CD40 SOD1	345 6647 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:10603	glucose intolerance Aliases: Glucose malabsorption Malabsorption of glucose	APOC3 CCL5 COQ2 HLA-DQA1 HNF1A HSPD1 LEP LEPR PON1 WFS1	27235 3117 3329 345 3952 3953 5444 6352 6927 7466	Homo sapiens (human)	Alliance of Genome Resources
DOID:1561	cognitive disorder Aliases: cognitive disease	APOC3 APP BDNF CHRFAM7A CHRNA7 COMT CSF3 DBN1 DMD EPHB2 GRIN1 GRIN2A GRIN2B HTR7 IL4 IRAK1 LAMP2 MAPT MMP3 MMP9 PPARG	1139 1312 1440 1627 1756 2048 2902 2903 2904 3363 345 351 3565 3654 3920 4137 4314 4318 5468 627 89832	Homo sapiens (human)	Alliance of Genome Resources
DOID:3145	hyperlipoproteinemia type III Aliases: Remnant hyperlipidemia carbohydrate induced hyperlipemia familial hypercholesterolaemia with hyperlipaemia familial type 3 hyperlipoproteinemia	APOC3 APOE	345 348	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111418	familial apolipoprotein C-II deficiency Aliases: C-II anapolipoproteinemia familial APOC2 deficiency familial apoC-II deficiency hyperlipoproteinemia, type 1b hyperlipoproteinemia, type Ib	APOC2	344	Homo sapiens (human)	Alliance of Genome Resources
DOID:14118	familial lipoprotein lipase deficiency Aliases: Fredrickson type I hyperlipoproteinemia Fredrickson type I lipaemia familial LPL deficiency familial hyperlipoproteinemia type I hypercholesterinaemic xanthomatosis hyperchylomicronemia mixed hyperglyceridemia	APOC2 LPL	344 4023	Homo sapiens (human)	Alliance of Genome Resources
DOID:3146	lipid metabolism disorder Aliases: dyslipidemia fatty acid metabolism disorder	APOC2 CPT1A CPT2 DHCR24 FADS2 HADHA HADHB HSD17B4 LEP LPIN1 LPIN2 LPIN3 MAT2A MVK NPY5R PPARA	1374 1376 1718 23175 3030 3032 3295 344 3952 4144 4598 4889 5465 64900 9415 9663	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111062	familial hypobetalipoproteinemia 1 Aliases: FHBL1	APOB	338	Homo sapiens (human)	Alliance of Genome Resources
DOID:4608	common bile duct neoplasm Aliases: neoplasm of common bile duct	APOB FSCN1 MSLN MTAP MUC1 MUC4 MUC5AC TYMP	10232 1890 338 4507 4582 4585 4586 6624	Homo sapiens (human)	Alliance of Genome Resources
DOID:4607	biliary tract cancer Aliases: malignant tumour of biliary tract	APOB CYP1A1 PPARD	1543 338 5467	Homo sapiens (human)	Alliance of Genome Resources
DOID:10923	sickle cell anemia Aliases: Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease sickle cell anaemia	APOB BCL11A C3 CD36 CD40LG CFB CYP2C19 F2 F3 GPX1 HBB HK1 HLA-DQB1 NOS3 NPPB PECAM1 PGF PON1 SPTA1 TGFB1 TNF	1557 2147 2152 2876 3043 3098 3119 338 4846 4879 5175 5228 53335 5444 629 6708 7040 7124 718 948 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:4606	bile duct cancer Aliases: Ca extrahepatic bile ducts bile duct tumor malignant neoplasm of the extrahepatic bile duct	APOB APOE TJP1	338 348 7082	Homo sapiens (human)	Alliance of Genome Resources
DOID:12241	beta thalassemia	APOB APOE BCL11A CFB COL1A1 HBB HBS1L HFE HLA-DQB1 HP IGFBP3 IL1A IL6 PON1 TERT TNF	10767 1277 3043 3077 3119 3240 338 348 3486 3552 3569 53335 5444 629 7015 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:1390	hypobetalipoproteinemia Aliases: Hypo-beta-lipoproteinemia	APOB APOC2 PCSK9	255738 338 344	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111421	familial apolipoprotein A5 deficiency Aliases: familial APOA5 deficiency familial apolipoprotein A-V deficiency	APOA5	116519	Homo sapiens (human)	Alliance of Genome Resources
DOID:1171	hyperlipoproteinemia type V Aliases: Fredrickson type V lipaemia familial hyperlipoproteinemia type V familial type 5 hyperlipoproteinemia	APOA5	116519	Homo sapiens (human)	Alliance of Genome Resources

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