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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 **3926 - 3950** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:6126	anal canal carcinoma Aliases: anal canal and Perianal gland carcinoma	SMUG1	23583	Homo sapiens (human)
DOID:8893	psoriasis	ACACA ACE ACO1 ACOT8 ADH1B AKR1B10 AKR1C1 AKR1C3 ALDH2 ALOX12 ALOX15 ALOX15B APRT B3GNT2 B3GNTL1 BST2 CAT CD14 CD1D CD38 CD93 CDH13 CHI3L1 CHST8 CLC CLEC16A CLEC7A CNTN3 COG6 COMT CS CYP1A1 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2E1 CYP3A4 DAG1 DLAT ELOVL6 FABP5 FAM20B FCGR3B FCN2 FUT2 GAL3ST2 GAPDH GBA1 GPX1 HPGDS HPSE ICAM1 ICAM5 IL18R1 IL1R1 IL1RAP IL1RL2 IPMK ISYNA1 ITLN1 KLRC1 LGALS1 LGALS3 LYNX1 LYZ MASP2 MBL2 MGAT5 MICA MRC1 MSMO1 NAGLU NAMPT NANS NCAM1 NT5E OLR1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PLA2G10 PLA2G1B PLA2G2A PLA2G7 PLB1 PLCD1 PSAP PTEN PTGS1 QTRT1 RBP4 RENBP SDC1 SELE SELP SFTPD SLC17A5 SMUG1 SOAT1 SPHK1 SPHK2 SPTLC2 ST6GAL1 STS SULF2 TLR2 TLR4 TNF UGT8 VCAM1 VNN1 VNN2 YDJC	10005 100507436 1012 10135 10678 10747 10855 1116 1178 125 1312 142 1431 146712 150223 151056 1543 1555 1557 1571 1576 1591 1593 1594 1605 1636 1645 1737 217 2171 2215 2220 22918 23274 23583 239 246 247 2524 253430 2597 2629 26503 27306 2876 31 3383 353 3554 3556 3821 3956 3958 4069 412 4153 4249 4360 4669 4684 48 4907 4973 5067 51477 5290 5291 5293 5294 5310 5319 5320 5333 54187 55600 55959 5660 56848 57016 5728 5742 57511 5950 5973 6307 6382 6401 6403 64090 64377 6441 64581 6480 66004 6646 684 7087 7097 7099 7124 7368 7412 79071 7941 81890 8399 847 8644 8808 8809 8875 8876 8877 912 929 9517 952 9917	Homo sapiens (human)
DOID:0050789	tarsal-carpal coalition syndrome	ABO ALOX5 CD44 CDH13 CYB5R3 GAPDH GLB1 HPGDS MRC1 NEU1 PLAUR PRSS8 PTEN PTGS2 TM7SF2 TNKS UPP2	1012 151531 1727 240 2597 2720 27306 28 4360 4758 5329 5652 5728 5743 7108 8658 960	Homo sapiens (human)
DOID:10393	secondary hypertrophic osteoarthropathy Aliases: Bamberger-Marie disease HPOA - hypertrophic pulmonary osteoarthropathy Marie Bamberger disease hypertrophic pulmonary osteoarthropathy	CBR1 CD55 DPEP1 PTEN PTGS2 SFTPA1 SFTPA2 SFTPC	1604 1800 5728 5743 6440 653509 729238 873	Homo sapiens (human)
DOID:1607	hypoglycemic coma	ACADM GCK HADH HMGCL	2645 3033 3155 34	Homo sapiens (human)
DOID:0080633	developmental cardiac valvular defect	PLD1 PLD2	5337 5338	Homo sapiens (human)
DOID:9602	necrotizing fasciitis	GALNS RECK	2588 8434	Homo sapiens (human)
DOID:4448	macular degeneration Aliases: Macular degeneration of retina	ACAT1 ACE ACO1 AKR1A1 ALDH3A2 ALDH5A1 ATP6AP2 B3GLCT BAD CALR CAT CD55 CHI3L1 CHST6 CYP1A2 CYP21A2 CYP24A1 CYP27A1 CYP2C19 CYP2R1 CYP46A1 ELOVL4 FADS1 FADS2 FCGR3B FCN2 FMOD FUT6 G6PD GALNS GPX3 HPGDS HS3ST4 HSD11B1 HSPG2 ICAM1 LGALS1 LIPC LPL MAN2B1 MASP1 MBL2 MUTYH NCAM1 OGG1 PARP12 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G12A PLCG2 PNPLA2 PPARGC1A PPT1 PTEN RENBP RPE SCD5 SELE SELL SELP SMUG1 SUCLA2 TLR4 UGT2B17 UNG XYLT1 XYLT2	10159 10327 10858 10891 1116 120227 142 145173 1544 1557 1589 1591 1593 1604 1636 2215 2220 224 2331 23583 2528 2539 2588 27306 2878 3290 3339 3383 38 3956 3990 3992 4023 4125 4153 4166 4595 4684 48 4968 5290 5291 5293 5294 5336 5538 5648 57104 572 5728 5973 6120 6401 6402 6403 64131 64132 64761 6785 7099 7367 7374 7915 79966 811 81579 847 8803 9415 9951	Homo sapiens (human)
DOID:0060400	chromosome 16p12.2-p11.2 deletion syndrome Aliases: 16p11.2-p12.2 microdeletion syndrome 16p11.2p12.2 microdeletion syndrome	CYP11A1 FREM1 PAFAH1B1 PRNP	1583 158326 5048 5621	Homo sapiens (human)
DOID:230	lateral sclerosis Aliases: adult-onset primary lateral sclerosis primary lateral sclerosis	ACHE APRT ASAH1 CAT CLEC10A FCN2 FIG4 GAL3ST1 GFRA1 HEXB HK2 NT5E OGA PNPLA6 SARM1 SLC35A1 TIGAR TMED9	10462 10559 10724 10908 2220 23098 2674 3074 3099 353 427 43 4907 54732 57103 847 9514 9896	Homo sapiens (human)
DOID:9352	type 2 diabetes mellitus Aliases: NIDDM insulin resistance non-insulin-dependent diabetes mellitus type 2 diabetes type II diabetes mellitus	ABO ACACA ACACB ACAT1 ACE ACHE ACLY ACOT2 ACOT7 ACSL1 ACSS2 ADH1B ADH1C ADIPOQ ADRB3 AGA AGPAT2 AKR1A1 AKR1B10 AKR1B1 AKR1C2 AKR1D1 AKT1 AKT2 ALDH2 ALDH6A1 ALDH7A1 ALDOB ALG1 ALOX12 ALOX5 ALPI ALPL ALPP AMACR AMY1A AMY1B AMY1C AMY2A ANXA5 APOD APRT ARSA ASAH2 ATP6AP2 ATRNL1 B4GALT5 BAAT BAD C1GALT1 CA4 CALR CANX CAT CBR1 CBR3 CD14 CD1D CD33 CD38 CD44 CD48 CD55 CDH13 CEACAM5 CEACAM7 CEL CERS2 CERS6 CH25H CHAT CHGA CHI3L1 CHIT1 CHPT1 CHST3 CLEC16A CLEC1B COG2 COL9A2 COLEC12 COMT CPT1A CPT2 CRTC2 CS CYB5R4 CYP11A1 CYP11B2 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP21A2 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP2E1 CYP2J2 CYP2R1 CYP3A4 CYP3A5 CYP46A1 CYP4F3 CYP7A1 CYP7B1 CYP8B1 DAG1 DCN DDOST DEGS1 DEGS2 DGAT1 DGCR2 DGKB DGKD DGKQ DGKZ DHCR7 DLAT DLD DSE DSEL EBP ELOVL3 ELOVL4 ELOVL5 ELOVL6 ENO1 ENO2 ENPP1 EPHX2 EXT1 EXT2 FADS1 FADS2 FASN FBP1 FCGR3B FCN3 FDPS FOLR2 FUCA1 FUT2 G6PC1 G6PC2 G6PD GAD1 GAD2 GAL3ST1 GALNS GALNT2 GALNT3 GAPDH GAS1 GCK GFPT1 GFPT2 GGT1 GHRL GK GLA GLB1 GLO1 GLUL GNPDA2 GNPNAT1 GPAT4 GPC5 GPD1 GPD2 GPI GPIHBP1 GPX1 GPX3 GSK3B GUSB GYG1 GYS1 H6PD HACD1 HADH HADHA HAS2 HAS3 HGSNAT HK1 HK2 HPGDS HPSE HS6ST1 HS6ST3 HSD11B1 HSD11B2 HSD17B12 HSD17B3 HSD17B6 HSD17B7 HSD3B1 HSPG2 ICAM1 IDH3A IDH3B IGF2 IGF2R IL18R1 IL1R1 IMPA1 INPP5F INPPL1 INS IRS2 ISYNA1 ITLN1 ITPK1 KCNJ11 KCNQ1 KL KLB KLRK1 L1CAM LARGE1 LDHA LEP LEPR LGALS1 LGALS3 LGALS4 LIPA LIPC LIPG LPIN1 LPIN2 LPL LY75 LYPLA1 LYZ MAN1A1 MAN2A1 MASP1 MASP2 MBL2 MBOAT7 MCAT ME1 MGAM MGAT2 MGAT4A MGAT4C MGLL MICA MIOX MLYCD MOGAT2 MPG MPI MRC1 MSMO1 MTM1 MTMR3 MUTYH NAAA NAGLU NAMPT NANS NCAM1 NDST1 NEIL1 NR1D1 OGA OGG1 OGT OLR1 OXCT1 PAPSS2 PARP1 PARP2 PC PCK1 PCK2 PCYT1A PCYT1B PDHB PDHX PDX1 PEMT PFKFB2 PFKFB3 PFKM PGM1 PGP PHOSPHO1 PIK3C2A PIK3C2G PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1B PKD1 PKLR PKM PLA2G10 PLA2G15 PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLAUR PLB1 PLCB3 PLCD1 PLCG1 PLD1 PMM2 PNLIP PNPLA2 PNPLA3 PNPLA6 POMGNT1 PPARD PPARGC1A PPP1CA PPP1CC PPP1R3A PPP1R3B PPP1R3C PRKAA1 PRKAA2 PRSS21 PRSS8 PSMD10 PTEN PTGDS PTGES2 PTGIS PTGS1 PTGS2 PYGB RBP4 REG1B REG3G RENBP RFT1 RPE RPN2 RTN4RL1 SACM1L SCD5 SCD SDC1 SDC2 SDC4 SDHA SDHB SELE SELL SELP SERPINA12 SFTPD SGMS1 SI SIGLEC1 SIGLEC5 SIGLEC7 SIRT2 SIRT4 SIRT6 SLC17A5 SLC2A10 SLC2A12 SLC2A1 SLC2A2 SLC2A3 SLC2A4 SLC2A5 SLC33A1 SLC35A1 SLC35B3 SLC35G1 SLC37A4 SLC39A8 SLC3A1 SLC5A1 SMPD1 SMUG1 SOAT1 SORD SPHK1 SPHK2 SPTLC1 SRD5A1 SRD5A2 SRGN ST3GAL3 ST3GAL4 ST6GAL1 ST6GALNAC3 ST8SIA4 STS SUCLA2 SULF2 SULT1E1 TALDO1 THEM4 TKFC TKT TKTL1 TKTL2 TLR4 TM7SF2 TNF TNKS2 TREH TYMP UCP2 UGCG UGGT2 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B15 UMOD UPP1 UPP2 VCAM1 VTCN1 XYLT1 XYLT2	10038 100507436 1012 10135 10159 10327 10400 10434 1048 10555 10558 10559 1056 10682 10724 10747 10855 10858 1087 10891 10908 10942 10965 1103 1113 1116 1118 11181 11320 11332 11343 117145 120227 123099 125 126 1298 130120 1312 132789 1374 1376 137964 138050 142 1431 145264 146760 151056 151531 152831 154091 1543 1544 1545 155 1555 1557 1558 1559 1571 1573 1576 1577 1581 1582 1583 1585 1586 1588 1589 1591 1593 159371 1594 1604 1605 1607 1609 162466 1634 1636 1646 1650 1717 1737 1738 175 1890 200186 2023 2026 2053 207 208 2131 2132 217 2180 2194 2203 2215 2224 2262 22796 22876 229 22908 22914 22933 231 23175 23274 23409 23417 2350 23583 23600 23659 239 240 248 249 250 2517 2524 253782 2538 2539 2542 256435 2571 2572 25834 2588 2590 2591 259230 2597 26007 26033 2619 2645 26503 266722 2673 2678 27036 2710 27163 2717 2720 27306 27349 2739 2752 276 277 278 279 28 2819 2820 2821 283871 2876 2878 2932 2990 2992 29940 29956 2997 3030 3033 3037 3038 308 3098 3099 31 32 3283 3290 3291 3293 3339 3340 3383 338328 3419 3420 347 3481 3482 353 3554 3612 3630 3636 3651 3705 3767 3784 38 3897 3939 3952 3953 3956 3958 3960 3988 3990 3992 4023 4051 4065 4069 410 412 4121 4124 4153 4199 4247 43 4329 4350 4351 4360 4534 4595 4669 4684 47 4968 4973 501 5019 5091 51000 5105 5106 51144 51167 51266 5130 51477 51478 51548 5162 5167 51738 5208 5209 5213 5236 5286 5288 5289 5290 5291 5293 5294 5310 5313 5315 5320 5321 5329 5331 5333 5335 5337 5373 5406 54187 54575 54576 54577 54578 54579 54600 54657 54658 54659 5467 5499 5501 5506 5507 5552 55586 55600 5562 55624 5563 55757 55902 55959 56052 5648 5652 56624 56848 56913 56994 570 57016 57104 5716 572 5728 5730 5740 5742 5743 57818 5834 5950 5968 5973 60481 6120 6185 6307 6319 6382 6383 6385 6389 6390 6401 6402 6403 64116 64131 64132 6441 6476 6480 6484 64841 6487 6513 6514 6515 6517 6518 6519 6523 6609 6614 6646 6652 6715 6716 6718 6783 6785 6888 7086 7099 7108 7124 7351 7357 7366 7369 7378 7412 762 7903 79071 79143 7941 79660 79661 79679 79966 80142 80168 80339 80351 8050 81031 81035 811 821 8277 83401 8395 8398 8399 84076 847 8473 8525 8527 8547 8560 8630 8660 8694 873 874 8778 8803 8809 8877 8897 8972 9023 9060 912 91869 9197 9200 92126 9215 929 9334 9365 9370 9388 9394 9415 9420 945 9468 9469 9514 952 9563 9572 960 962 9663 9945 9993	Homo sapiens (human)
DOID:7400	Nijmegen breakage syndrome Aliases: Berlin breakage syndrome Microcephaly, normal intelligence and immunodeficiency NBS Seemanova syndrome II Seemanova syndrome type 2 ataxia-telangiectasia variant immunodeficiency-microcephaly-chromosomal instability syndrome microcephaly-immunodeficiency-lymphoreticuloma syndrome	IDH1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN TMED3	142 23423 3417 5290 5291 5293 5294 5728	Homo sapiens (human)
DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type Aliases: EBS-gen sev EBSDM epidermolysis bullosa herpetiformis Dowling-Meara type epidermolysis bullosa simplex, herpetiformis generalized severe epidermolysis bullosa simplex	PLOD3	8985	Homo sapiens (human)
DOID:0110570	autosomal dominant nonsyndromic deafness 47 Aliases: DFNA47 autosomal dominant deafness 47	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)
DOID:0080822	aspirin-induced respiratory disease Aliases: aspirin-sensitive asthma	PTGS2	5743	Homo sapiens (human)
DOID:0050850	diabetic encephalopathy	GSK3B	2932	Homo sapiens (human)
DOID:0050523	adult T-cell leukemia/lymphoma Aliases: Adult T-cell leukemia/lymphoma (HTLV-1 positive) adult T-cell leukemia	APRT CAT CD38 CD44 CNTN2 CYP1A1 ENO2 FCGR3B FUT4 ICAM1 LCT LGALS1 LGALS3 LGALS9 MRC1 MTAP NAMPT NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PLCG1 PSMD10 PTEN RENBP SACM1L SELL SOAT1 TIGAR TMED5 TMED9 VCAM1	10135 1543 2026 2215 22908 2526 3383 353 3938 3956 3958 3965 4360 4507 4684 50999 5290 5291 5293 5294 5335 54732 57103 5716 5728 5973 6402 6646 6900 7412 847 952 960	Homo sapiens (human)
DOID:0060294	cold-induced sweating syndrome Aliases: Crisponi syndrome Sohar-Crisponi syndrome	CNTFR	1271	Homo sapiens (human)
DOID:13711	dental fluorosis Aliases: Intrinsic enamel discolouration of fluorosis Mottled teeth Mottling of enamel	ACAN COMT HPGDS MMP25	1312 176 27306 64386	Homo sapiens (human)
DOID:12919	Plasmodium ovale malaria Aliases: Malariaby Plasmodium ovale Ovale malaria	G6PD	2539	Homo sapiens (human)
DOID:3039	cecum adenocarcinoma Aliases: Cecal adenocarcinoma	NT5E	4907	Homo sapiens (human)
DOID:0050453	lissencephaly	ALPP ATP6V0A2 ATP6V1A ATRNL1 B3GALNT2 B4GAT1 CD33 CD38 COMT CRPPA CYP2B6 DAG1 DHCR24 DLD DLST FCN2 FIG4 FKRP FKTN HSPG2 LARGE1 NSDHL OCRL PAFAH1B1 PIGA PIGN PIGP PIGQ PLCB1 PLCE1 PLCG1 POMGNT1 POMGNT2 POMK POMT1 POMT2 PTEN RXYLT1 SDC2 SLC17A5 STS TMTC3	10329 10585 11041 1312 148789 1555 160418 1605 1718 1738 1743 2218 2220 23236 23545 23556 250 26033 26503 29954 3339 412 4952 5048 50814 51196 51227 523 5277 5335 55624 5728 6383 729920 79147 84197 84892 9091 9215 945 952 9896	Homo sapiens (human)
DOID:2712	phimosis Aliases: Tight foreskin Tight frenulum	CYP1A1 CYP1B1 CYP27B1 SRD5A2	1543 1545 1594 6716	Homo sapiens (human)
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	ACE AMACR ARSA CANX CAT CD44 CYP4F3 DGAT2 FIG4 GBA1 GPX2 HADHB HK1 HPSE LCAT LPIN1 MAG MTM1 MTMR2 PGK1 PGM1 PLCB4 PLCE1 PRNP PRPS1 PTGS2 SIGLEC7 SPTLC1 SPTLC2	10558 10855 1636 23175 23600 2629 27036 2877 3032 3098 3931 4051 4099 410 4534 51196 5230 5236 5332 5621 5631 5743 821 84649 847 8898 9517 960 9896	Homo sapiens (human)
DOID:0060791	hypomyelinating leukodystrophy 9 Aliases: HLD9 RARS-related autosomal recessive hypomyelinating leukodystrophy	GBA1	2629	Homo sapiens (human)

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