GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **3151 - 3175** of **7942** in total

« First

‹ Prev

…

123

124

125

126

127

128

129

130

131

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:2043	hepatitis B Aliases: chronic hepatitis B hepatitis B infection	ABO ACACA ACE ACOD1 ADH1B AKR1A1 AKR1B10 ALDH2 ALDH3A2 ALOX5 ANXA5 APRT ARSA BCKDHB BST2 CALR CAT CD14 CD1D CD209 CD44 CEACAM5 CHI3L1 CHKA CLEC7A CYP17A1 CYP1A2 CYP21A2 CYP27B1 CYP2B6 CYP2C19 CYP2E1 CYP2R1 CYP3A4 DGAT2 EBP ENO1 ENOSF1 EXT1 FASN FCGR3B FCN2 G6PD GAL3ST1 GALNT10 GAPDH GBA1 GFPT1 GGT1 GLB1 GOLPH3 GPC3 GPI GUSB GYS2 HACD1 HK2 HMMR HPGDS HPSE2 HPSE HS3ST3B1 HS6ST3 HSD17B8 HSPG2 ICAM1 IGF2R IL18R1 IL1RL1 INPPL1 ISYNA1 KLRB1 KLRC1 KLRD1 KLRK1 LGALS3 LGALS4 LGALS9 LIPA LY75 LYPD5 MBL2 MBOAT7 MGAT3 MICA MPI MPPE1 MRC1 NAMPT NANS NCAM1 OGG1 PAPSS1 PARP1 PCYT1A PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PLAUR PLCE1 PLPP1 PNPLA3 PRKAA2 PRKCSH PRNP PRSS21 PSAP PSMD10 PTEN PTGES PTGS2 RGN SDC2 SELE SHMT2 SIGLEC1 SIRT2 SLC17A5 SLC35A1 SLC35A2 SOAT1 SPHK1 SRGN TDG TKT TKTL1 TMED5 TNF UAP1 UGT1A1 UGT1A6 UGT1A7 UNG VCAN VTCN1 XYLT2 YDJC	100507436 10135 10327 1048 10559 10682 10855 10942 1116 1119 120227 125 142 1462 150223 1544 1555 1557 1571 1576 1586 1589 1594 1636 2023 2131 217 2194 2215 2220 224 22914 22933 240 2539 2597 2629 26503 266722 2673 2678 2719 2720 27306 28 2821 284348 2923 2990 2998 308 30835 3099 31 3161 3339 3383 3482 353 3636 3820 3821 3824 3958 3960 3965 3988 4065 410 4153 4248 4351 4360 4684 4968 50999 51196 5130 51477 5290 5291 5293 5294 5320 5329 54187 54577 54578 54658 5552 55556 55568 5563 5589 5621 5660 57016 5716 5728 5743 594 60495 6383 6401 64083 64132 64581 6472 65258 6614 6646 6675 684 6996 7086 7124 730249 7355 7374 79143 7923 79679 80339 811 8277 84649 847 8611 8809 8877 9061 9104 912 9173 9200 929 9514 9536 960 9953	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:12549	hepatitis A Aliases: Viral hepatitis, type A	ACE ACOT7 AKR1D1 ALDH2 CALR CAT CD1D COLGALT2 CYP19A1 CYP27A1 CYP2B6 CYP2C19 CYP2C9 CYP2E1 DLAT ECHS1 EXT1 FUT8 G6PD GOLPH3 GPC3 HAS1 HAS3 HPGDS KLRB1 KLRC1 KLRK1 LGALS1 LGALS3 LGALS9 MICA MRC1 NAMPT NCAM1 OGG1 PARP1 PARP2 PTGES PTGS2 SGMS1 SLC17A5 TIPARP TNF UGT1A1 UMOD	10038 100507436 10135 11332 142 1555 1557 1559 1571 1588 1593 1636 1737 1892 2131 217 22914 23127 2530 2539 259230 25976 26503 2719 27306 3036 3038 3820 3821 3956 3958 3965 4360 4684 4968 54658 5743 64083 6718 7124 7369 811 847 912 9536	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0080177	hepatic veno-occlusive disease Aliases: veno-occlusive disease	CD22 FCN2 HPSE TYMP XYLT2	10855 1890 2220 64132 933	Homo sapiens (human)	DisGeNET
DOID:11512	Budd-Chiari syndrome Aliases: hepatic vein thrombosis	CALR CD55 CYP2C9 GPLD1 PIGM	1559 1604 2822 811 93183	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12550	hepatic coma Aliases: Hepatocerebral intoxication	CD14 DLD G6PD GLUL ISYNA1 PCK1 PTGS1 SMUG1 STS	1738 23583 2539 2752 412 5105 51477 5742 929	Homo sapiens (human)	DisGeNET DisGeNET
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	CD14 DLD G6PD GLUL ISYNA1 PCK1 PTGS1 SMUG1 STS	1738 23583 2539 2752 412 5105 51477 5742 929	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:12119	hemosiderosis Aliases: haemosiderosis	ACSM3	6296	Homo sapiens (human)	DisGeNET
DOID:9746	hemorrhoid Aliases: hemorrhoidal disease	ADH1C ALDH2 CYP1A1 ENO1	126 1543 2023 217	Homo sapiens (human)	DisGeNET
DOID:11266	Hantavirus hemorrhagic fever with renal syndrome Aliases: HFRS Hemorrhagic fever, Russian Hemorrhagic nephrosonephritis Puumala virus nephropathy	BAAT CAT CHI3L1 ICAM2 IL1R1 IL1RL1 LGALS3 MBD4 MRC1 MUTYH NAAA PTGS1 PTGS2 SLC35D3 TM7SF2 VCAM1	1116 27163 3384 340146 3554 3958 4360 4595 570 5742 5743 7108 7412 847 8930 9173	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:12287	Crimean-Congo hemorrhagic fever Aliases: CHF Congo virus Congo-Crimean Hemorrhagic Fever Crimean hemorrhagic fever	CAT ICAM1 SLC17A5	26503 3383 847	Homo sapiens (human)	DisGeNET
DOID:12134	factor VIII deficiency Aliases: Congenital factor VIII disorder Hemophilia A Subhemophilia classic hemophilia A	ABO FUT1 G6PD GUSB HPSE2 LMAN1 MCFD2 MRC1 PRNP	2523 2539 28 2990 3998 4360 5621 60495 90411	Homo sapiens (human)	DisGeNET DisGeNET
DOID:11482	hemopericardium Aliases: Haemopericardium	ACADVL ACE ALG9 CAT GBA1 PMM2 PTGS2 SMUG1	1636 23583 2629 37 5373 5743 79796 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	A4GALT ABO BAAT C1GALT1C1 CAT CD22 CLEC1B CYP21A2 DGKE G6PD GPI GRHPR IL1RL1 LIPG MASP1 MBL2 PIGA PLA2G7 SLC35G1 ST8SIA2 TM7SF2	1589 159371 2539 28 2821 29071 4153 51266 5277 53947 5648 570 7108 7941 8128 847 8526 9173 933 9380 9388	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:582	hemoglobinuria	G6PD PIGA	2539 5277	Homo sapiens (human)	DisGeNET
DOID:5379	hemoglobin E disease Aliases: Hb-E disease	ABO FUT1 G6PD NT5E SCD UGT1A1	2523 2539 28 4907 54658 6319	Homo sapiens (human)	DisGeNET
DOID:5378	hemoglobin D disease Aliases: Hb-D disease	ABO FUT1 G6PD NT5E SCD UGT1A1	2523 2539 28 4907 54658 6319	Homo sapiens (human)	DisGeNET
DOID:2859	hemoglobin C disease Aliases: Hb-C disease	ABO FUT1 G6PD NT5E SCD UGT1A1	2523 2539 28 4907 54658 6319	Homo sapiens (human)	DisGeNET
DOID:2351	iron metabolism disease Aliases: disorder of iron metabolism iron disorder	ACACA ACE ACO1 AKR1D1 ALPP ANXA5 ARSA ATRNL1 CALR CAT CCDC115 CYP27B1 G6PD GALNS GLUL GNPAT GPX1 HJV IL1R1 NDUFAB1 PNPLA3 PRNP SLC17A5 SLC39A8 SMPD1 VCAM1	148738 1594 1636 250 2539 2588 26033 26503 2752 2876 308 31 3554 410 4706 48 5621 64116 6609 6718 7412 80339 811 84317 8443 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:2352	hemochromatosis Aliases: Haemochromatosis diabetes bronze iron storage disorder	ACACA ACE ACO1 AKR1B1 AKR1D1 ALDH2 ALPP ANXA5 ARSA ATRNL1 CALR CAT CCDC115 CD14 CYP27B1 FADS2 FUT1 FUT2 G6PD GALNS GLUL GNPAT GPC1 GPC3 GPC5 GPX1 HJV HPGDS ICAM1 IL1R1 LGALS3 NDUFAB1 PIK3CA PIK3CB PIK3CD PIK3CG PNPLA3 PRNP RGMA RGMB SELE SELL SLC17A5 SLC39A8 SMPD1 STS SULT1E1 TNF TUSC3 UGT1A1 VCAM1	148738 1594 1636 217 2262 231 250 2523 2524 2539 2588 26033 26503 2719 27306 2752 2817 285704 2876 308 31 3383 3554 3958 410 412 4706 48 5290 5291 5293 5294 54658 5621 56963 6401 6402 64116 6609 6718 6783 7124 7412 7991 80339 811 84317 8443 847 929 9415	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	ACACA ACE ACO1 AKR1D1 ALPP ANXA5 ARSA ATRNL1 CALR CAT CCDC115 CYP27B1 G6PD GALNS GLUL GNPAT GPX1 HJV IL1R1 NDUFAB1 PNPLA3 PRNP SLC17A5 SLC39A8 SMPD1 VCAM1	148738 1594 1636 250 2539 2588 26033 26503 2752 2876 308 31 3554 410 4706 48 5621 64116 6609 6718 7412 80339 811 84317 8443 847	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:8499	night blindness Aliases: nyctalopia	ARSG CA4 CACNA2D4 COG4 ELOVL4 HADHA HGSNAT HK1 HSD3B7 NYX PCYT1A POMGNT1	138050 22901 25839 3030 3098 5130 55624 60506 6785 762 80270 93589	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:74	hematopoietic system disease Aliases: Blood disease Blood dyscrasia DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS Hematological disease blood disorder disease of haematopoietic system disease of hematopoietic system haematopoietic system disease	ALPP ATRNL1 CALR CLEC1B CYP2J2 FUT1 G6PD GOLPH3 HPRT1 ICAM5 IDH2 IL18R1 LMAN1 MCFD2 PIGA PIK3CD PKLR POGLUT1 SMUG1 SOAT1 UGT1A1	1573 23583 250 2523 2539 26033 3251 3418 3998 51266 5277 5293 5313 54658 56983 64083 6646 7087 811 8809 90411	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0001816	angiosarcoma Aliases: hemangiosarcoma	DCN ICAM1 PIK3CA PIK3CB PIK3CD PIK3CG PLCG1 PTEN SMUG1 TP53	1634 23583 3383 5290 5291 5293 5294 5335 5728 7157	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:2725	capillary hemangioma Aliases: Capillary haemangioma Congenital vascular hamartoma Congenital vascular naevus Infantile hemangioma Juvenile hemangioma Strawberry haemangioma Strawberry nevus Strawberry nevus of skin cellular hemangioma of Infancy	ACE ATP6AP2 ATP6V1A C1GALT1C1 CYP1B1 GNPTAB MAG MTM1 MTMR14 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SDHC SDHD SRD5A3	10159 1545 1636 29071 4099 4534 523 5290 5291 5293 5294 5728 6391 6392 64419 79158 79644	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:474	histiocytoid hemangioma Aliases: Angiolymphoid hyperplasia with eosinophilia epithelioid haemangioma epithelioid hemangioma	C1GALT1C1 CALR CD14 CTSA DPM1 GAS1 GPC6 HSD17B2 IDH1 IDH2 IGF2R IL18R1 LGALS9 MAG PIGF PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PNPLA2 PNPLA6 PTEN SDHD	10082 10908 2619 29071 3294 3417 3418 3482 3965 4099 5281 5290 5291 5293 5294 5310 5476 57104 5728 6392 811 8809 8813 929	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements