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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 **1426 - 1450** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:3963	thyroid gland carcinoma Aliases: head and neck cancer, Thyroid	ABO ACACA ACE AGK AGPS AKR1C2 ALOX12 ALOX15 AMACR ANXA5 APRT ARSA ASAH1 BAAT CAT CD1D CD44 CD74 CD93 CEACAM5 CNTN1 CYB5R3 CYP19A1 CYP1A1 CYP24A1 CYP27B1 CYP2B6 CYP3A4 DCN DPEP1 ENPP2 FH FUCA1 G6PD GAPDH GFRA1 GLB1 GPC3 GPD2 GPLD1 GPX1 GPX3 GUSB HPGDS HPRT1 HPSE HSPG2 ICAM1 IDH1 IDH2 IDUA IGF2R IL1R1 INPP4B KL KLB L1CAM LDHA LGALS16 LGALS1 LGALS3 MBL2 MICA MINPP1 MRC1 MUTYH NAMPT NCAM1 NTHL1 PARP1 PARP4 PFKFB3 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2R1 PRKAA2 PTEN PTGDS PTGES2 PTGES3 PTGS1 PTGS2 QPRT RECK RPIA SCD SDC1 SDC2 SDC4 SDHB SDHC SDHD SIRT4 SLC2A3 SMUG1 SOAT1 SORD SPHK1 TKTL1 ULBP2 UPP1 VCAN VTCN1	100507436 10135 1048 10728 10855 1272 142 143 1462 148003 152831 1543 1555 1576 1588 1591 1594 1634 1636 1646 1727 1800 2271 22918 22925 22934 23409 23475 23583 23600 239 246 2517 2539 2597 2674 2719 2720 27306 28 2820 2822 2876 2878 2990 308 31 3251 3339 3383 3417 3418 3425 3482 353 3554 3897 3939 3956 3958 410 4153 427 4360 4595 4684 4913 5168 5209 5290 5291 5293 5294 5315 5563 55750 570 5728 5730 5742 5743 6319 6382 6383 6385 6390 6391 6392 6515 6646 6652 7378 79679 80142 80328 8277 8434 847 8540 8821 8877 912 9365 9562 960 972	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:9312	chronic ethmoiditis Aliases: chronic ethmoid sinusitis chronic ethmoidal sinusitis ethmoidal sinusitis - chronic	CHI3L1 CLC CYP11A1 CYP11B1 HPGDS HPSE HSD11B1 HSD11B2 ICAM1 IL1RL1 LYZ PGM3 PLB1 PTGDS PTGS1 SELE SFTPA1 SFTPD	10855 1116 1178 151056 1583 1584 27306 3290 3291 3383 4069 5238 5730 5742 6401 6441 653509 9173	Homo sapiens (human)	DisGeNET
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	ACACA ACE ACHE ACO1 ACO2 ACOT7 ACSBG1 ADH1B ADH1C ADH4 ADH7 AKR1A1 AKT1 AKT2 ALDH2 ANXA5 APRT ARSA ASAH1 ATP6AP2 B3GALT4 B3GAT1 B4GALNT1 BST1 CALR3 CALR CAT CD14 CD38 CD44 CD55 CEACAM6 CEL CHAT CHI3L1 CHIT1 CNTN1 CNTN2 COMT CTNS CYP17A1 CYP1A1 CYP1A2 CYP1B1 CYP27B1 CYP2B6 CYP2C19 CYP2C9 CYP2E1 CYP3A5 CYP4F3 DCN DGKD DHRS11 DLD DPEP1 ELOVL7 ENO2 EPHX2 FASN FBP1 FBXO2 FCER2 FCGR3B FH G6PD GAD1 GAD2 GALC GALNS GAPDH GBA1 GBA2 GFPT1 GLA GLB1 GLUL GNPDA2 GPI GPNMB GPX1 GSK3B GSTO1 GSTO2 HAS2 HEXA HK1 HK2 HPGDS HSD17B6 HSD17B7 HSD3B7 ICAM1 IDUA IGF2 IGF2R INPP5F INPP5K ISYNA1 KL L1CAM LEP LGALS1 LGALS3 LGALS4 LYPD5 MAG MAPK14 MCAT MDGA2 MGLL MRC1 NAGLU NEIL1 NT5E NTM OGA OGG1 PAFAH1B1 PARP1 PDHA1 PDIA3 PGK1 PGK2 PGP PIGC PIK3C2B PIK3CA PIK3CB PIK3CD PIK3CG PISD PKD1 PLA2G1B PLA2G6 PLB1 PLD1 PLD2 PNPLA6 PPARGC1A PRKAA1 PRKAA2 PRNP PSAP PTEN PTGDS PTGES3 PTGES PTGIS PTGS2 RENBP RGMA RTN4R SARM1 SCD SDHA SHMT1 SHMT2 SI SIGLEC7 SIRT2 SLC17A5 SLC2A4 SLC33A1 SLC39A8 SMPD1 SMPD2 SMPD3 SMUG1 SOAT1 SPTSSB ST3GAL2 ST8SIA4 STBD1 SUCLA2 SYNJ1 SYNJ2 TALDO1 TIGAR TKT TM7SF2 TMED9 TNKS2 UGT1A9 UMOD VCAM1 XYLT2	10159 10327 10457 1056 10724 10728 10891 10908 1103 1116 1118 11332 11343 119391 125 125972 126 127 1272 131 1312 132789 142 1432 1497 151056 1543 1544 1545 1555 1557 1559 1571 1577 1586 1594 1604 161357 1634 1636 165679 1738 1800 2026 2053 207 208 217 2194 2203 2208 2215 2271 22876 22933 23098 23205 23583 23761 2539 2571 2572 2581 2583 2588 2597 26232 2629 26503 2673 27036 27087 2717 2720 27306 27349 2752 2821 283871 284348 2876 2923 2932 3037 3073 308 3098 3099 31 3383 3425 3481 3482 353 3897 3952 3956 3958 3960 4051 4099 410 427 43 4360 4669 4680 48 4907 4968 50 5048 50863 51477 51478 5160 51763 5230 5232 5279 5287 5290 5291 5293 5294 5310 5319 5337 5338 54600 54732 55512 5562 5563 5621 5660 56963 57103 5728 5730 5740 5743 57704 5973 6319 6389 64116 64132 6470 6472 6476 6483 65078 6517 6609 6610 6646 683 6888 6900 7086 7108 7369 7412 7903 79154 79661 79993 80270 80351 811 8398 847 8527 8630 8705 8803 8867 8871 8987 9197 929 9365 9446 952 9536 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:5139	cellular leiomyoma	LDHA	3939	Homo sapiens (human)	DisGeNET
DOID:0111344	myeloproliferative disorder with eosinophilia Aliases: chronic myeloproliferative disorder with eosinophilia	ALPP ANXA5 ATRNL1 B3GAT1 CEACAM5 CEACAM7 COMT DCN ENO2 FCGR3B ICAM1 LTA4H NCAM1 PKM SCD SMUG1 TKT VTCN1	1048 1087 1312 1634 2026 2215 23583 250 26033 27087 308 3383 4048 4684 5315 6319 7086 79679	Homo sapiens (human)	DisGeNET
DOID:26	pancreas disease	ACE ALDH2 CEL CYP2E1 MSLN PLA2G2A PRPS1 PTEN	10232 1056 1571 1636 217 5320 5631 5728	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0110553	autosomal dominant nonsyndromic deafness 23 Aliases: DFNA23 autosomal dominant deafness 23	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)	DisGeNET
DOID:0050891	adrenal cortical adenoma Aliases: adrenocortical adenoma	CYP11B1 CYP11B2	1584 1585	Homo sapiens (human)	Alliance of Genome Resources
DOID:104	bacterial infectious disease	ACE ACOT7 AKR1C4 ALOX5 ANXA5 APRT ATP6AP2 CALR CAT CD14 CD1D CD55 CEACAM5 CEACAM6 CEL CH25H CHI3L1 CLEC7A COLEC11 CYP27B1 ENO1 FCN2 FCN3 HJV ICAM1 IL18R1 IL1RAP ITLN1 KL KLRD1 LYZ MASP1 MBL2 OGG1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G10 PLA2G1B PLA2G2A PLA2G4A PLB1 PRKAA2 PTEN PTGS2 RENBP SDC1 SDC4 SIRT2 SLC27A5 SLC35A2 SLC5A1 SMUG1 STS TUSC3 XYLT2	10159 1048 1056 10998 1109 1116 11332 148738 151056 1594 1604 1636 2023 2220 22933 23583 240 308 3383 353 3556 3824 4069 412 4153 4680 4968 5290 5291 5293 5294 5319 5320 5321 55600 5563 5648 5728 5743 5973 6382 6385 64132 64581 6523 7355 78989 7991 811 83666 8399 847 8547 8809 9023 912 929 9365	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0090071	hypogonadotropic hypogonadism 11 with or without anosmia	ACSM3 ADH5 CD44 CD55 CYP17A1 CYP19A1 GAS1 GK GPC1 HJV HS6ST1 HSD17B3 L1CAM MMUT NT5E PMM2 PNPLA6 SEMA7A SMPD3 SOAT1 STS TYMP	10908 128 148738 1586 1588 1604 1890 2619 2710 2817 3293 3897 412 4594 4907 5373 55512 6296 6646 8482 9394 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0111633	congenital sucrase-isomaltase deficiency Aliases: CSID SI deficiency congenital sucrase-isomaltose malabsorption congenital sucrose intolerance disaccharide intolerance	SI	6476	Homo sapiens (human)	Alliance of Genome Resources
DOID:1858	McCune Albright syndrome Aliases: fibrous dysplasia of bone osteitis fibrosa disseminata polyostotic fibrous dysplasia	ACSS2 AMY1A AMY1B AMY1C APRT ENPP1 PLA2G15 SUCLG1	23659 276 277 278 353 5167 55902 8802	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:1443	cerebral degeneration Aliases: Brain degeneration	ABO ACACA ACADVL ACAT1 ACE ACER3 ACHE ACO1 ACO2 ACOT7 ACOT8 ACSL6 ACSS2 ADH1B ADPRS AGA AGPS AGRN AKR1A1 AKR1C2 AKR1C4 ALDH2 ALDH7A1 ALG11 ALG13 ALG1 ALG3 ALOX12 ALOX5 ALPI ALPP ANXA5 APRT ARSA ASAH1 ATP6AP2 ATP6V1A ATRNL1 B3GALNT2 B3GALT4 B3GAT1 B3GLCT BCAN BST1 CALR CAT CD14 CD177 CD209 CD33 CD38 CD44 CD55 CD74 CDH13 CEACAM5 CEACAM6 CFC1 CH25H CHAT CHI3L1 CHIT1 CLC CLEC16A CLEC1B CLEC7A CLN5 CNTN1 CNTN2 COG1 COG4 COG5 COG6 COG7 COLGALT1 COLGALT2 COMT CPO CPT1A CRYL1 CS CSPG4 CTNS CYP11A1 CYP17A1 CYP19A1 CYP1A2 CYP27A1 CYP2B6 CYP2C9 CYP2J2 CYP3A4 CYP46A1 CYP7B1 CYP8B1 DCN DEGS1 DGKQ DHCR24 DHDDS DHRS11 DLD DLST DPEP2 DSE EDEM2 EFNA5 ENO1 ENO2 ENPP2 EPHX2 EPM2A EXT1 EXT2 FASN FBXO2 FCGR3B FCN2 FDPS FH FOLR2 FUCA1 G6PD GAD1 GAD2 GALNS GAPDH GAPDHS GBA1 GBA2 GFRA1 GGT1 GLB1 GLO1 GLUL GM2A GNE GNPAT GNPDA2 GOLPH3 GPAA1 GPC1 GPC6 GPI GPNMB GPX1 GTDC1 GUSB HAS1 HAS3 HK1 HMGCS2 HPGDS HPSE2 HPSE HS3ST1 HSD11B1 HSD17B1 HSD17B4 HSD17B6 HSD17B7 HSPG2 HYI ICAM1 IDH1 IDH2 IGF2R IL1R1 IL1RAP IL1RL1 IMPA1 INPP5D INPP5K INPPL1 ITPKB KL KLRC1 L1CAM LCAT LCT LDHA LGALS3 LGALS4 LGALS9 LIPA LIPC LIPG LMAN2L LPL LTC4S LYZ LYZL4 MAG MAN1B1 MAN2B1 MASP1 MBL2 MBOAT7 MDH2 MELTF MGAT3 MGLL MICA MMUT MOGAT3 MOGS MPDU1 MPG MPI MRC1 NAAA NAGA NAMPT NANP NANS NCAM1 NDST1 NEU1 NGLY1 NPL NT5E OGA OGDH OGDHL OGG1 OGT OLR1 PAFAH1B2 PARP1 PC PCCA PCCB PCK1 PCYT1A PCYT1B PCYT2 PDHA1 PEMT PFKFB3 PGAP1 PGD PGP PI4KA PIGC PIGG PIGL PIGN PIGT PIGU PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIKFYVE PKM PLA2G15 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLAUR PLB1 PLCB1 PLCG2 PLD1 PLD2 PLD3 PLPP4 PMM2 PNP PNPLA2 PNPLA7 PPT1 PRG2 PRKAA2 PRNP PTDSS1 PTEN PTGDS PTGES2 PTGES3 PTGES PTGS1 PTGS2 RENBP RGN RTN4R SCD5 SCD SCP2 SDC2 SDC3 SDCBP2 SFTPA1 SFTPC SGMS2 SGSH SI SIGLEC7 SIRT2 SIRT6 SLC17A5 SLC2A3 SLC2A4 SLC33A1 SLC35A1 SLC35A2 SMPD2 SMPD3 SMUG1 SOAT1 SPHK1 SPHK2 SQLE ST3GAL3 ST3GAL4 ST6GAL1 ST8SIA1 STS SUCLA2 SUCLG1 SUCLG2 SUMF1 SYNJ1 TECR TIGAR TKT TM7SF2 TMED9 TPI1 TUSC3 UGCG UGT1A1 UMOD UNG VCAM1 VCAN	10005 10020 100507436 10082 1012 10135 10159 10195 10327 10400 10457 10466 1048 10559 10724 10728 10855 10858 1103 1109 1116 1118 11253 11332 11343 1178 1203 125 1272 128869 130749 1312 131375 132789 1374 140838 142 1431 145173 1462 1464 148789 1497 151056 1544 1555 1559 1573 1576 1582 1583 1586 1588 1593 1604 1609 1634 1636 1646 166929 1718 1738 1743 175 1946 196051 200576 2023 2026 2053 2131 2132 217 2194 2215 2220 2224 2271 22933 23127 23236 23274 23305 2350 23556 23583 23646 23659 239 240 248 250 2517 2539 2571 2572 25839 2588 2597 26033 26232 2629 26330 26503 2674 2678 27036 27087 27111 27163 2720 27306 2739 2752 2760 28 2817 2821 283871 285362 2876 2990 29940 3036 3038 308 30835 3098 31 3158 3290 3292 3295 3339 3340 3383 3417 3418 346606 3482 353 3554 3556 3612 3635 3636 37 3707 375775 375790 38 3821 3897 3931 3938 3939 3958 3960 3965 3988 3990 4023 4056 4069 4099 410 412 4125 4153 4191 4241 4248 427 43 4350 4351 4360 440138 4594 4668 4680 4684 4758 48 4860 4907 4967 4968 4973 50 501 5049 5091 5095 5096 5105 51084 51266 5130 51478 51548 5160 51604 5168 51763 5209 5226 523 5279 5289 5290 5291 5293 5294 5297 5315 5319 5320 5321 5329 5336 5337 5338 5373 54187 54658 54732 54872 54936 55331 5538 55512 5553 5563 55741 55753 55768 55902 55997 56052 5621 5648 56848 57103 57104 57126 5728 5730 5742 5743 57511 57704 5833 5973 60495 6319 6342 63827 6383 64083 64174 6440 6448 64581 6476 6480 6484 6487 6489 65078 6515 6517 653509 6610 6646 6713 683 6900 7086 7108 7167 7355 7357 7369 7374 7412 7841 79143 79154 7941 7957 79709 79712 79868 7991 79947 79966 80055 80142 80896 811 81562 81888 8398 8443 847 8473 8540 8560 8630 8705 8733 8801 8802 8803 8867 8877 9023 9104 9173 91949 9197 929 9365 9382 9388 9420 945 9468 9487 952 9524 9526 9536 960 9672 972 9791 9957	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0111235	congenital muscular dystrophy-dystroglycanopathy type A12 Aliases: MDDGA12 Walker-Warburg syndrome or muscle-eye-brain disease POMK-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12	POMK	84197	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:3516	adult fibrosarcoma	ACE AKR1A1 AKR1B1 ANXA5 APRT CD44 CHST3 DLD EBP GLB1 GLO1 GPI HK1 HPRT1 HSPG2 IDH1 MMP25 MTAP NAMPT PARP1 PC PIK3CA PIK3CB PIK3CD PIK3CG PSAP PTGES3 PTGS2 SDC1 SDC2 SIGLEC7 SMPD1 STS	10135 10327 10682 10728 142 1636 1738 231 27036 2720 2739 2821 308 3098 3251 3339 3417 353 412 4507 5091 5290 5291 5293 5294 5660 5743 6382 6383 64386 6609 9469 960	Homo sapiens (human)	DisGeNET
DOID:0070238	primary coenzyme Q10 deficiency 1 Aliases: COQ10D1 CoQ deficiency 1 CoQ10 deficiency, primary, 1 coenzyme Q deficiency 1 ubiquinone deficiency 1	COQ2	27235	Homo sapiens (human)	Alliance of Genome Resources
DOID:1509	avoidant personality disorder Aliases: anxious personality disorder	COMT IMPA1	1312 3612	Homo sapiens (human)	DisGeNET
DOID:0050630	Aland Island eye disease Aliases: FORSIUS-ERIKSSON TYPE OCULAR ALBINISM Forsius-Eriksson syndrome	GK	2710	Homo sapiens (human)	DisGeNET
DOID:0060389	chromosome 10q23 deletion syndrome	MBL2 MUTYH PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGS2 SMUG1	23583 4153 4595 5290 5291 5293 5294 5728 5743	Homo sapiens (human)	DisGeNET
DOID:0111263	combined malonic and methylmalonic acidemia Aliases: CMAMMA combined malonic and methylmalonic aciduria	ACSF3	197322	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0060305	megalocornea Aliases: anterior megalophthalmos congenital anterior megalophthalmia	FKRP FKTN GMPPB GNPTAB LARGE1 POMGNT1 POMK POMT1 POMT2 SLC2A10	10585 2218 29925 29954 55624 79147 79158 81031 84197 9215	Homo sapiens (human)	DisGeNET
DOID:0060856	right atrial isomerism Aliases: Ivemark syndrome asplenia with cardiovascular anomalies	CFC1	55997	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060486	Perry syndrome Aliases: parkinsonism with alveolar hypoventilation and mental depression	HACD1	9200	Homo sapiens (human)	DisGeNET
DOID:2769	tic disorder	CD44 ENO2	2026 960	Homo sapiens (human)	DisGeNET DisGeNET
DOID:934	viral infectious disease Aliases: Viral Infection Viral disease virus infection	ABO ACACA ACACB ACE ACHE ACOD1 ACOT7 ACSBG1 AGPAT1 AKR1A1 AKR1C4 ALDH2 ALOX5 AMACR ANXA5 APRT ASAH1 ATP6AP2 B3GAT1 BST2 CALR CAT CD14 CD1D CD209 CD33 CD38 CD44 CD48 CD74 CEACAM5 CERS1 CHST10 CLEC10A CLEC1B CLEC5A CLEC9A COLEC11 CPT2 CSPG5 CYP2B6 CYP4F3 DDOST DLD ENPP1 FASN FBP1 FCGR3B FCN2 FUT2 G6PD GALNT3 GAPDH GGT1 GLB1 GLDC GOLPH3 GPC3 GPI HACD1 HK2 HPSE2 HPSE HSD17B6 ICAM1 IGF2R IL1RL1 INPP5D INPP5E ISYNA1 KLRB1 KLRC1 KLRK1 LDHA LGALS1 LGALS3 LGALS8 LGALS9 LY75 MASP2 MBL2 MGAM MICA MOGS MRC1 NAAA NAGLU NCAM1 OGDH PARP11 PARP12 PARP1 PCK2 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G6 PLAUR PLCB2 PLCE1 PNPLA3 PNPLA6 PRKAA2 PRNP PSMD10 PTEN PTGS1 PTGS2 RECK SCD SELE SFTPA1 SFTPD SI SIGLEC1 SIRT6 SLC17A5 SLC2A2 SLC35A1 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 STT3B TALDO1 TM7SF2 TPI1 VCAM1 XYLT2	100507436 10159 10327 10462 1048 10554 10559 10675 10715 10747 10855 10908 1109 11332 1376 142 1555 1636 1650 1738 201595 217 2194 2203 2215 2220 22914 23205 23583 23600 23601 240 2524 2539 2591 2597 26503 2678 27087 27163 2719 2720 2731 28 2821 283420 308 30835 3099 31 32 3383 3482 353 3635 3820 3821 3939 3956 3958 3964 3965 4051 4065 4153 427 43 4360 4669 4684 4967 5106 51196 51266 51477 51548 5167 5290 5291 5293 5294 5315 5329 5330 5563 5621 56623 56848 57097 5716 5728 5742 5743 60495 6319 6401 64083 64132 6441 6476 64761 6514 653509 6609 6614 6646 684 6888 7108 7167 730249 7412 7841 78989 80339 811 8398 8434 847 8630 8877 8972 912 9173 9200 929 945 9486 952 960 962 972	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET

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