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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	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **6576 - 6600** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:3635	congenital myasthenic syndrome	ACHE AGRN ALG14 ALG2 B3GAT1 CHAT DPAGT1 GFPT1 GMPPB SEMA7A SLC25A1	1103 1798 199857 2673 27087 29925 375790 43 6576 8482 85365	Homo sapiens (human)
DOID:11123	Henoch-Schoenlein purpura Aliases: Allergic purpura Autoimmune purpura Henoch-Sch?nlein purpura Henoch-Sch@nlein purpura Henoch-Scholein purpura Henoch-Schonlein Purpura Purpura, autoimmune	ACE B4GALNT1 C1GALT1 CPT1C CYP19A1 CYP2U1 CYP7B1 GBA2 ICAM1 L1CAM MBL2 MGAT5 NAAA PARP1 PLA2G6 PLD3 PNPLA6 SLC33A1	10908 113612 126129 142 1588 1636 23646 2583 27163 3383 3897 4153 4249 56913 57704 8398 9197 9420	Homo sapiens (human)
DOID:4914	esophagus adenocarcinoma Aliases: Oesophageal adenocarcinoma	AKR1A1 AKR1B10 AKR1C2 AMACR APRT CALR CD55 CDH13 CEACAM5 CEACAM7 CYP19A1 CYP1A1 CYP24A1 FASN GHRL GPX3 GPX7 HPGDS ICAM1 LGALS9 MCAT MPG MTAP PARP1 PIGA PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G4A PLB1 PLCE1 PTEN PTGES PTGS1 PTGS2 SLC35A2 SMUG1 STS TYMP UGT2B17 UGT8	1012 10327 1048 1087 142 151056 1543 1588 1591 1604 1646 1890 2194 23583 23600 27306 27349 2878 2882 3383 353 3965 412 4350 4507 51196 51738 5277 5290 5291 5293 5294 5319 5321 57016 5728 5742 5743 7355 7367 7368 811 9536	Homo sapiens (human)
DOID:0110771	hereditary spastic paraplegia 18 Aliases: IDMDC SPG18 autosomal recessive spastic paraplegia 18 autosomal recessive spastic paraplegia type 18 intellectual disability, motor dysfunction and joint contractures	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:0110809	hereditary spastic paraplegia 57 Aliases: SPG57 autosomal recessive spastic paraplegia 57 autosomal recessive spastic paraplegia type 57	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:1324	lung cancer	ABO ACACA ACAT1 ACE ACHE ACLY ACOT7 ACOT8 ACSBG1 ACSL1 ACSL3 ACSL4 ACSS1 ACSS2 ACYP2 ADH1A ADH1B ADH1C ADH5 ADH7 AGL AGRN AKR1A1 AKR1B10 AKR1B1 AKR1C1 AKR1C2 AKR1C3 ALDH1A3 ALDH1B1 ALDH2 ALDH3A1 ALDH3A2 ALDH7A1 ALDOA ALG13 ALG1 ALOX12B ALOX15 ALOX15B ALOX5 ALPI ALPP AMACR AMY1A AMY1B AMY1C ANXA4 ANXA5 APRT ARSA ARSF ASAH1 ATP6AP2 ATRNL1 B3GALNT1 B3GAT1 B3GNT3 B3GNTL1 B4GALT1 BAAT BPHL BRAF BST1 CA4 CACNA2D2 CALR CANX CAT CBR1 CD109 CD14 CD177 CD1D CD22 CD33 CD38 CD44 CD55 CD74 CD93 CDH13 CEACAM5 CEACAM6 CEACAM7 CEMIP CERS6 CHAT CHGA CHI3L1 CHKA CHKB CHODL CHPT1 CHST7 CLEC10A CLEC14A CNTN1 CNTN2 COMT CPM CRLS1 CRYBG3 CTSA CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP21A2 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP2E1 CYP2R1 CYP3A4 CYP3A5 CYP3A7-CYP3A51P CYP3A7 CYP4F3 DCN DDOST DGKA DGKH DHCR24 DHDDS DHDH DLD EBP EFNA1 ELOVL6 ENO1 ENO2 ENO3 ENPP1 ENPP2 EPHX2 ERLEC1 EXTL3 FASN FBP1 FBXO17 FCGR3B FCN2 FDFT1 FOLR1 FOLR2 FUT10 FUT11 FUT1 FUT2 FUT3 FUT4 FUT5 FUT7 FUT8 FUT9 G6PD GAD1 GALC GALK2 GALNS GALNT14 GALNT3 GALNT6 GAPDH GBE1 GCK GCNT1 GCNT3 GFPT2 GGT1 GLB1 GLCE GLDC GLUL GMDS GML GOLPH3 GPC1 GPC3 GPC5 GPI GPX1 GPX2 GPX3 GPX7 GUSB HADHA HAGH HAS2 HAS3 HK1 HK2 HKDC1 HMMR HPGDS HPRT1 HPSE HS3ST2 HS3ST3B1 HS6ST2 HSD11B1 HSD11B2 HSD17B1 HSD17B6 HSPG2 HYAL1 HYAL2 ICAM1 ICAM2 IDH1 IDH2 IDH3A IGF2R IL18R1 IL1RL1 IMPA1 INPP4A INPP4B INPP5D INPPL1 ISYNA1 ITPKA ITPKB KHK KL KLB KLRB1 KLRD1 KLRK1 L1CAM LAYN LDHA LDHB LDHC LGALS1 LGALS3 LGALS4 LGALS8 LGALS9 LIPC LPCAT1 LPIN1 LPIN3 LPL LY6K LYNX1 LYPD3 LYPD5 LYPLA1 MBD4 MBL2 MCAT MDH1 MDH2 ME1 ME2 MELTF MGLL MICA MMUT MOGS MPG MRC1 MSLN MTAP MTMR3 MUTYH NAMPT NCAM1 NEIL1 NEIL2 NEU1 NEU3 NT5E NTHL1 OGA OGG1 OLR1 OPCML PAFAH1B1 PAPSS1 PARG PARP1 PC PCK2 PCYT1A PDIA3 PFKFB3 PGAM1 PGD PGK1 PIGN PIK3C2B PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKD2 PKM PLA2G10 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLAUR PLB1 PLCB3 PLCB4 PLCD1 PLCE1 PLCG1 PLCH1 PLOD3 PLPP4 PLPP5 PMM2 PNPLA2 POFUT1 POGLUT1 PPT1 PRG2 PRKAA2 PRNP PRSS8 PSMD10 PTEN PTGES3 PTGES PTGIS PTGS1 PTGS2 PYGB QTRT1 RECK REG1B REG3G RENBP RGMB RGN RPN2 RTN4R SCD SDC1 SDC2 SDC4 SDHA SDHC SELE SELP SEMA7A SFTPA1 SFTPA2 SFTPC SFTPD SGMS1 SHMT1 SHMT2 SIGLEC9 SIRT2 SIRT4 SIRT6 SLC17A5 SLC26A2 SLC2A10 SLC2A3 SLC2A5 SLC33A1 SLC35A4 SLC5A1 SMC3 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 SQLE SRGN ST6GAL1 ST8SIA2 ST8SIA4 STS SULF1 SULF2 SULT1E1 SYNJ2 THEM4 TIGAR TM7SF2 TMTC3 TNFRSF10C TNKS2 TNKS TPI1 TPST1 TREH TUSC3 TYMP UGCG UGDH UGP2 UGT1A1 UGT1A3 UGT1A6 UGT1A7 UGT1A9 UGT2B17 UGT8 ULBP1 UMPS UNG VCAM1 VCAN VTCN1 XXYLT1 YDJC	10005 100507436 100861540 1012 10135 10159 10232 10327 10331 10434 10462 1048 10682 10690 10724 10728 10825 10855 1087 1103 1113 1116 11181 1119 1120 11226 11332 11343 113829 115290 117145 120227 124 125 126 1272 128 130120 131 1312 131544 135228 1368 140578 142 143903 1462 146712 150223 151056 152002 152831 1543 1544 1545 1551 1555 1557 1558 1559 1571 1576 1577 1586 1588 1589 1591 1593 1594 1604 160418 1606 160851 161198 1634 1636 1645 1646 1650 170384 1718 1738 178 1836 1890 1942 196051 2023 2026 2027 2053 2137 217 218 2180 2181 2182 219 2194 220 2203 2215 2220 2222 224 226 2262 22914 22918 22933 23007 231 23175 23205 23213 23409 2348 2350 23509 23556 23583 23600 240 242 246 247 248 250 2523 2524 2525 2526 2527 2529 252969 2530 253782 2539 2571 2581 2585 2588 2591 259230 2597 26033 26035 2632 2645 2650 26503 2678 2683 27076 27087 27180 2719 2720 27248 27294 27306 2731 27349 2752 276 2762 2765 277 278 28 2817 2821 284348 285704 2876 2877 2878 2882 2923 2990 3029 3030 3037 3038 307 308 3098 3099 31 3161 3251 3290 3291 3292 3339 3373 3383 3384 3417 3418 3419 3482 353 3612 3631 3635 3636 3706 3707 375790 3795 38 3820 3824 3897 3939 3945 3948 3956 3958 3960 3964 3965 3990 4023 4051 410 412 4153 416 4190 4191 4199 4200 4241 427 43 4350 4360 4507 4594 4595 4680 4684 47 4758 4907 4913 4968 4973 4978 501 5048 5091 5106 51196 5130 51477 51548 5167 5168 5209 5223 5226 5230 5287 5289 5290 5291 5293 5294 5310 5311 5315 5319 5320 5321 5329 5331 5332 5333 5335 5373 54577 54578 54600 54658 54659 54675 54742 5476 5538 5552 5553 5563 55902 55959 56052 5621 5652 56548 56848 56983 56994 570 57016 57103 57104 57126 5716 57214 5728 5740 5742 5743 5834 5968 5973 6185 6319 6382 6383 6385 6389 6391 6401 6403 64083 6440 6441 6470 6472 6480 64900 65078 6515 6518 6523 653509 66004 6609 6646 670 6713 673 6783 683 6900 7108 7167 729238 7357 7358 7360 7367 7368 7372 7374 7412 762 7841 7903 79071 79623 79661 79679 79868 79888 7991 79947 80201 80329 80351 81031 811 8128 81890 821 8398 8399 8434 84513 84532 8460 847 84750 8482 8505 8630 8644 8658 8692 8706 873 8794 8809 8821 8871 8877 8897 8930 8985 90161 9061 9104 912 9126 9173 9197 9245 9254 929 933 9365 945 952 9536 960 972 98 9945 9953 9956	Homo sapiens (human)
DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2 Aliases: CVPT2	ACADVL ACE CALR CHPT1 FKRP FUT1 GOLPH3 GYG1 PTGS2 SCD	1636 2523 2992 37 56994 5743 6319 64083 79147 811	Homo sapiens (human)
DOID:1407	anterior uveitis	LACC1 TLR2 TLR4 TNF	144811 7097 7099 7124	Homo sapiens (human)
DOID:6067	ovarian mucinous neoplasm Aliases: Ovarian mucinous tumor malignant ovarian mucinous neoplasm mucinous tumor of Ovary	PDHX PTEN	5728 8050	Homo sapiens (human)
DOID:1059	intellectual disability	ACAT1 ACER3 ACHE ACSL4 ADPRS AGA AGPAT2 AGRN ALDH3A2 ALDH5A1 ALDH7A1 ALDOB ALG11 ALG13 ALG14 ALG2 ALG9 ALOX12B AMT AMY1A AMY1B AMY1C ARSA ARSD ARSI ASAH1 ATP6AP2 ATP6V0A2 ATP6V1A B3GALNT2 B3GALT6 B3GLCT B4GALNT1 BCKDHA BCKDHB CA4 CACNA2D1 CALR CAT CD38 CERS1 CHAT CHKB CLN5 CMAS CNTN2 CNTN4 CNTN6 COG5 COG6 COG8 COLEC10 COLEC11 COMT CRPPA CTSA CYB5R3 CYP24A1 CYP27A1 CYP2U1 DAG1 DBT DCN DGCR2 DHCR24 DHCR7 DLD DPAGT1 EBP ENOSF1 EOGT EPM2A EXT1 EXT2 EXTL3 FASN FBP1 FCN2 FCSK FDFT1 FKRP FKTN FUCA1 FUT8 G6PC3 G6PD GAD1 GALT GAS1 GBA2 GBE1 GCK GCSH GGT1 GK GLB1 GLDC GLYCTK GMPPA GMPPB GNPAT GNPTAB GNS GPAA1 GPC3 GPC6 GPD2 GPI GUSB HACD1 HADH HADHA HADHB HEXA HGSNAT HK1 HMGCL HPRT1 HS6ST2 HSD17B12 IDH1 IDH2 IDH3A IDH3B IDS IDUA IL1RAP IL1RAPL1 IMPA1 INPP5E INPP5K IRS2 KDSR KL L1CAM L2HGDH LARGE1 LDHA LDHD LFNG LSS MACROD2 MAG MAN1B1 MAN2B1 MAN2C1 MANBA MASP1 MBOAT7 MMUT NAGA NAGLU NANS NDST1 NDST2 NDST3 NDST4 NEU1 NSDHL NTNG1 OCRL OGT PAFAH1B1 PAFAH1B3 PAPSS2 PARP1 PC PCCA PCCB PCYT1A PDHA1 PDHX PDIA3 PGAP1 PGAP2 PGAP3 PGK1 PGM3 PIGA PIGB PIGC PIGG PIGL PIGN PIGO PIGP PIGQ PIGU PIGV PIGW PIK3CA PIK3CB PIK3CD PIK3CG PLCH2 PMM2 PNP PNPLA6 POMGNT1 POMGNT2 POMK POMT1 POMT2 PPT1 PRPS1 PTDSS1 PTEN RENBP RXYLT1 SC5D SDHA SDHB SDHC SDHD SGSH SLC17A5 SLC2A10 SLC33A1 SLC35A1 SLC35A2 SLC35A3 SLC39A8 SMC3 SRD5A3 ST3GAL3 ST3GAL5 STS STT3B SUCLG1 SULT1E1 SUMF1 SYNJ1 TECR TKT TMTC3 TNFRSF10C TPI1 TUSC3 TYMP UGCG UMPS XYLT1 XYLT2	10082 10159 10329 10466 10555 10559 10584 10585 10682 10715 10908 1103 11141 1120 11253 113612 1203 126792 128869 1312 132158 138050 140733 142 145173 148789 152330 1591 1593 160418 1605 1629 1634 1717 1718 1727 1738 175 1798 1890 197257 197258 199857 201595 2131 2132 2137 2182 2194 2203 2218 2220 2222 224 22854 229 23443 23545 23556 242 2517 2530 2531 2539 2571 2583 2592 2619 2632 2645 26503 2653 2678 2710 2719 2720 27255 2731 27315 275 276 277 278 2799 2820 2821 284098 285203 285362 2923 2990 29925 29926 29954 3030 3032 3033 3073 3098 3155 3251 3340 340075 3417 3418 3419 3420 3423 3425 3556 3612 375790 38 3897 3939 3955 4047 4099 410 412 4123 4125 4126 414 427 43 440138 4594 4668 4669 4758 4860 4952 501 5048 5050 50814 5091 5095 5096 51144 51227 5130 5160 51763 523 5230 5238 5277 5279 5290 5291 5293 5294 5373 54187 5476 54872 54936 55331 5538 55556 55624 55650 55907 5631 5648 56623 5728 57511 57704 593 594 5973 6309 6389 6390 6391 6392 64116 64131 64132 6448 64579 6487 6783 6900 7086 7167 729920 7355 7357 7372 762 781 78989 79143 79147 7915 79158 7957 79644 79796 79868 7991 79944 80055 8050 81031 811 84197 84342 8443 847 84720 8473 84892 8509 85365 8660 8733 8794 8802 8867 8869 90161 9060 9091 9126 9197 9200 9215 92579 93210 9348 9365 9487 9488 952 9524 9651 9791 9993	Homo sapiens (human)
DOID:0080411	familial adenomatous polyposis 3	NTHL1	4913	Homo sapiens (human)
DOID:12506	Bell's palsy Aliases: Bell palsy Bell's (facial) palsy	ACADS ACSL4 AGRN ALG13 ALG14 ALG2 ASAH1 CHKB DPAGT1 FKRP GFPT1 GMPPB GNE HPGDS IL1RAPL1 LARGE1 MTM1 MTMR14 MTMR2 POMT1 POMT2 PTDSS1 SMUG1	10020 10585 11141 1120 1798 199857 2182 23583 2673 27306 29925 29954 35 375790 427 4534 64419 79147 79868 85365 8898 9215 9791	Homo sapiens (human)
DOID:10024	migraine with aura Aliases: classic migraine	ACE ATP1A2 CAT PMM2	1636 477 5373 847	Homo sapiens (human)
DOID:0060889	prune belly syndrome Aliases: Eagle-Barret syndrome Obrisnksy syndrome abdominal muscle deficiency syndrome	ACAN ALDH2 DGCR2 ICAM1 MRC1 PARP1 PTGS2 SELE SFTPD SMC3	142 176 217 3383 4360 5743 6401 6441 9126 9993	Homo sapiens (human)
DOID:724	female stress incontinence Aliases: Stress incontinence - female female urinary stress incontinence	ACOT7 ARSA CAT DCN FMOD GBA1 GPI	11332 1634 2331 2629 2821 410 847	Homo sapiens (human)
DOID:0110579	autosomal dominant nonsyndromic deafness 53 Aliases: DFNA53 autosomal dominant deafness 53	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:3602	toxic encephalopathy Aliases: neurotoxicity neurotoxicity syndrome	CAT CYP3A5 PTGES3 ST8SIA1	10728 1577 6489 847	Homo sapiens (human)
DOID:0070146	hereditary sensory neuropathy type 4 Aliases: hereditary sensory neuropathy type IV insensitivity to pain, congenital, with anhidrosis	PKLR SPTLC1	10558 5313	Homo sapiens (human)
DOID:1974	adenosarcoma Aliases: mullerian Adenosarcoma	AKR1C3 ANXA5 APRT CALR CAT CD14 CD38 CD44 CDH13 CEACAM5 CRLS1 CYP19A1 CYP27B1 ENO2 EXT2 FH FUT4 GAPDH GPC3 GUSB HPGDS IGF2R MRC1 MSLN NCAM1 OGG1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLCE1 PLCG2 PNPLA2 PTEN PTGS2 QPRT RECK SHMT1 SLC2A3 SRD5A2	1012 10232 1048 142 1588 1594 2026 2132 2271 23475 2526 2597 2719 27306 2990 308 3482 353 4360 4684 4968 51196 5290 5291 5293 5294 5336 54675 57104 5728 5743 6470 6515 6716 811 8434 847 8644 929 952 960	Homo sapiens (human)
DOID:0110781	hereditary spastic paraplegia 30 Aliases: SPG30 autosomal spastic paraplegia type 30	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:12177	common variable immunodeficiency Aliases: CVID acquired agammaglobulinemia acquired hypogammaglobulinemia common variable agammaglobulinemia sporadic hypogammaglobulinemia	CD14 CD1D CD38 CDH13 CHIT1 CLEC16A DAG1 FCGR3B FCN2 FUT2 IL18R1 MBL2 MRC1 NCAM1 NEIL1 PIK3CD SDC1 SMUG1	1012 1118 1605 2215 2220 23274 23583 2524 4153 4360 4684 5293 6382 79661 8809 912 929 952	Homo sapiens (human)
DOID:10970	spastic quadriplegic cerebral palsy Aliases: inherited congenital spastic quadriplegia inherited congenital spastic tetraplegia quadriplegic infantile cerebral palsy spastic quadriplegia tetraplegic infantile cerebral palsy	ACHE ACSM1 ACSM2A ALDH3A2 ALPP ARSA ARSD ATRNL1 CAT CD109 CYP24A1 CYP3A4 EFNA5 GAD1 GCDH GLUL GMDS GPX1 HPRT1 IDH1 IDH2 IDUA MBL2 MECR MRC1 PDHA1 PIK3CA PIK3CB PIK3CD PIK3CG PMM2 PNP PTGS1 PTGS2 RENBP SOAT1 ST3GAL5 TIGAR TKTL1 UGT1A1	116285 123876 135228 1576 1591 1946 224 250 2571 26033 2639 2752 2762 2876 3251 3417 3418 3425 410 414 4153 43 4360 4860 51102 5160 5290 5291 5293 5294 5373 54658 57103 5742 5743 5973 6646 8277 847 8869	Homo sapiens (human)
DOID:4447	cystoid macular edema	ACE CALR CAT	1636 811 847	Homo sapiens (human)
DOID:12155	lymphocytic choriomeningitis Aliases: LCM Lymphocytic choriomeningitis virus encephalomyelitis Lymphocytic meningitis Lymphocytic meningoencephalitis	CD44 CHAT CLEC12A DAG1 SELL	1103 160364 1605 6402 960	Homo sapiens (human)
DOID:0090055	dystonia 25	ALDH5A1	7915	Homo sapiens (human)

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