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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 **6626 - 6650** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:12028	Conn's syndrome Aliases: Conn syndrome primary aldosteronism	ATP6AP2 CD44 CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP21A2 CYP4F3 G6PD HSD11B2 HSD3B1 HSD3B2 LGALS3 OCRL PRSS8 PTGS2 SLC26A2 SLC33A1 SLC5A1	10159 1583 1584 1585 1586 1589 1836 2539 3283 3284 3291 3958 4051 4952 5652 5743 6523 9197 9469 960	Homo sapiens (human)
DOID:0050465	Muir-Torre syndrome	MRC1 MUTYH	4360 4595	Homo sapiens (human)
DOID:12165	retinal lattice degeneration Aliases: Palisade degeneration of retina	RPE	6120	Homo sapiens (human)
DOID:14755	argininosuccinic aciduria Aliases: Argininosuccinate lyase deficiency argininosuccinic acidemia arginosuccinase deficiency deficiency of argininosuccinate lyase	ARSA ARSD RGN	410 414 9104	Homo sapiens (human)
DOID:5419	schizophrenia Aliases: schizophrenia-1	ABO ACACA ACADS ACAN ACE ACHE ACO2 ACOT7 ACSL4 ACSL6 ACSM1 ADH5 AGA AKR1A1 AKT1 ALDH2 ALDH3A1 ALDH3B1 ALDH7A1 ALDOC ALG1 ALG9 ALOX12 ALPL AMACR AMY1A APRT ARSA ARSD ARSG ASAH1 ATP6V1A B3GAT1 B3GAT2 B3GNT2 CACNA2D3 CALR CAT CD14 CD38 CD48 CDH13 CERK CFC1 CHAT CHGA CHI3L1 CHPT1 CHST10 CHST11 CHST3 CHST9 CLEC10A CNTN2 CNTN4 CNTN5 CNTN6 COMT CRLS1 CSPG4 CSPG5 CYP19A1 CYP1A2 CYP21A2 CYP2B6 CYP2C19 CYP2C9 CYP2E1 CYP3A4 CYP3A5 CYP4F3 DEGS2 DGCR2 DGKH DGKI DGKZ DHDDS DLD EBP EDEM2 EFNA5 ELOVL5 ENO2 EPHX2 EPM2A ETNPPL EXT1 FADS1 FADS2 FBP1 FCN2 FH FUCA2 FUT11 FUT8 G6PD GAD1 GAD2 GALC GALNT10 GALNT2 GAPDH GBA1 GCSH GFRA1 GFRA2 GLDC GLO1 GLT8D1 GLUL GLYCTK GNPAT GPC1 GPC6 GPX1 GSK3B GTDC1 GUSB HAGH HK1 HK2 HPGDS HS3ST5 HS6ST1 HSD11B2 HSD17B12 HSPG2 HTR2A ICAM1 IL18R1 IL1R1 IMPA2 INPP5A KL L1CAM LCT LGALS1 LGALS3 LIPC LMAN2L LPL MAG MAN1C1 MAN2A1 MAN2A2 MCAT MDGA1 MDH1 ME2 MECR MGAT1 MPI NCAM1 NCAN NDST3 NEU1 NPL NTM NTNG1 OGG1 OPCML PAFAH1B1 PARP1 PARP9 PCCB PCK1 PCYT1A PEMT PFKM PGK1 PGP PI4K2B PI4KA PIK3C2A PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PIP4K2C PLA2G10 PLA2G12A PLA2G15 PLA2G1B PLA2G2A PLA2G4A PLA2G4B PLA2G4C PLA2G4D PLA2G5 PLA2G6 PLA2G7 PLB1 PLCB1 PLCB4 PLCG1 PLCH2 PLPP1 PMM2 PNPLA2 POFUT1 POFUT2 PPARA PPT1 PRNP PSAP PSMD10 PTEN PTGDS PTGES3 PTGIS PTGS1 PTGS2 RBKS RENBP RFT1 RPN2 RTN4R SCD SDHA SELL SHMT1 SHMT2 SLC27A5 SLC2A3 SLC35G1 SLC39A8 SMPD3 SMUG1 SPTLC1 SRD5A2 ST3GAL1 ST3GAL3 ST6GALNAC1 ST8SIA2 ST8SIA3 ST8SIA4 STS STT3A SULT1E1 SUMF1 TBXAS1 TIGAR TKT TMED5 TMTC1 TNF TPI1 TUSC3 UGT1A3 UGT1A8 UXS1 VCAM1	100137049 10082 1012 10327 10400 10462 10558 10675 10678 10682 10728 10998 1103 1113 1116 11332 116285 123099 128 1312 132158 135152 142 1463 1464 151056 152330 1544 1555 1557 1559 1571 1576 1577 1588 1589 159371 160851 1636 170384 1738 175 176 1946 2026 2053 207 2131 217 218 2182 2203 221 2220 222537 2271 22854 22901 230 23236 23275 23305 23509 23583 23600 23659 239 249 2519 2530 2539 2571 2572 2581 2590 2597 2629 2653 266727 2674 2675 27087 27255 27306 2731 27349 2739 2752 276 28 2817 283748 283871 285362 2876 2932 2990 3029 3098 3099 31 3291 3339 3356 3383 35 353 3554 3613 3632 3703 3897 3938 3956 3958 3990 3992 4023 4051 4099 410 412 4122 4124 414 4190 4200 4245 427 43 4351 4684 4758 4968 4978 50 501 5048 50515 50863 5096 50999 51046 5105 51102 51144 5130 5213 523 5230 5286 5289 5290 5291 5293 5294 5297 5305 5319 5320 5321 5322 5332 5335 5373 53942 54576 5465 54659 54675 55300 5538 55512 55568 55741 55799 55808 55830 55997 56052 5621 5660 56994 57103 57104 57134 5716 5728 5730 5740 5742 5743 5973 60481 6185 6319 6389 6402 64080 64116 6470 6472 64781 6482 64850 6487 65078 6515 6716 6783 6900 6916 7086 7124 7167 7412 7903 7941 7957 79712 79796 79837 7991 79947 80146 80896 811 8128 81562 81579 83539 83666 83857 8398 8399 8443 847 8525 8605 8611 8809 9162 91869 929 9348 9365 9394 9415 9469 9486 952 962 9651 9993	Homo sapiens (human)
DOID:5062	phencyclidine abuse Aliases: PCP abuse	FDFT1	2222	Homo sapiens (human)
DOID:5403	microcystic adenoma	ACACA ACE ACSL4 ADH1C AKR1B10 AKR1B1 ALDH2 ALOX12 ALOX5 AMACR APRT ARSA BAAT CALR CD44 CD74 CDH13 CEACAM5 CEACAM6 CEACAM7 CEMIP CHGA CHI3L1 CHPT1 CHST3 CYP11A1 CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP21A2 CYP24A1 CYP2C9 CYP2E1 CYP3A5 DHCR24 DLD DPEP1 ENO2 ENPP7 FUT4 FUT8 G6PC1 GALNT12 GFRA2 GLUL GPC3 GPNMB GPX1 GPX2 GUSB HPGDS HPSE HSD11B1 HSD11B2 HSD17B1 HSD17B7 HSD3B1 HSPG2 IDH1 IGF2R KL LGALS1 LGALS3 LGALS4 LMAN1 LYZ MBD4 MGAT5 MGLL MPG MRC1 MTAP MUTYH NAGLU NAMPT NCAM1 NTHL1 OGG1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTEN PTGIS PTGS1 PTGS2 QPRT SDC2 SDHC SELL SHMT1 SLC26A2 SLC2A3 SLC33A1 SMUG1 SORD SPHK1 UGT1A1 UGT1A6 VCAN	1012 10135 10457 1048 10855 1087 1113 1116 11343 126 142 1462 1543 1544 1545 1559 1571 1577 1583 1584 1585 1586 1588 1589 1591 1636 1718 1738 1800 1836 2026 217 2182 231 23475 23583 23600 239 240 2526 2530 2538 2675 2719 27306 2752 2876 2877 2990 31 3283 3290 3291 3292 3339 339221 3417 3482 353 3956 3958 3960 3998 4069 410 4249 4350 4360 4507 4595 4669 4680 4684 4913 4968 51478 5290 5291 5293 5294 54578 54658 56994 570 57016 5716 57214 5728 5740 5742 5743 6383 6391 6402 6470 6515 6652 79695 811 8877 8930 9197 9365 9469 960 972	Homo sapiens (human)
DOID:5556	testicular malignant germ cell cancer Aliases: malignant germ cell tumor of testis	CYP1A1 CYP2B6 CYP3A5 CYP3A7 HPGDS PSMD10 SMUG1	1543 1551 1555 1577 23583 27306 5716	Homo sapiens (human)
DOID:14766	renal agenesis Aliases: hereditary renal aplasia hereditary urogenital adysplasia renal adysplasia renal aplasia	FKRP FKTN FREM1 GFRA1 GPC3 LARGE1 PIGN PIGP PIGQ POMT1 POMT2 SLC2A4	10585 158326 2218 23556 2674 2719 29954 51227 6517 79147 9091 9215	Homo sapiens (human)
DOID:643	progressive multifocal leukoencephalopathy	ARSF CAT CD14 GAD1 HPGDS PARP1 PLAUR PRNP PSAP SCP2 SOAT1	142 2571 27306 416 5329 5621 5660 6342 6646 847 929	Homo sapiens (human)
DOID:0110106	atrial heart septal defect 1 Aliases: ASD1 atrial septal defect 1	ACADVL ALG12 ARSA ARSD ATP6V1A B3GALT6 B3GAT3 B3GLCT CAT CFC1 CHST14 CHST3 COMT CYP11A1 CYP11B2 CYP1B1 CYP2E1 DSE FIG4 FKTN G6PC3 GAA GPC3 GPC6 MASP1 MMUT PCYT1A PIGA PIGN PIGQ PLD1 PTEN RENBP SMC3 TALDO1 TGDS TKT XYLT2	10082 113189 126792 1312 145173 1545 1571 1583 1585 2218 23483 23556 2548 26229 2719 29940 37 410 414 4594 5130 523 5277 5337 55997 5648 5728 5973 64132 6888 7086 79087 847 9091 9126 92579 9469 9896	Homo sapiens (human)
DOID:14239	gastrointestinal tularemia Aliases: Enteric tularemia intestinal tularaemia	MBL2	4153	Homo sapiens (human)
DOID:8478	actinomycosis Aliases: Actinomycotic madura foot Actinomycotic mycetema Actinomycotic mycetoma of foot Madura foot due to Actinomadura actinomycotic infection	CAT	847	Homo sapiens (human)
DOID:0060475	myoclonic-atonic epilepsy Aliases: EEOC childhood onset epileptic encephalopathy	SLC25A10	1468	Homo sapiens (human)
DOID:0110351	osteogenesis imperfecta type 11 Aliases: OI11 osteogenesis imperfecta type XI	ALPL BAAT CD38 CD44 DCN PNPLA2 PTGS2 SMPD3	1634 249 55512 570 57104 5743 952 960	Homo sapiens (human)
DOID:3744	cervical squamous cell carcinoma Aliases: squamous cell carcinoma of cervix squamous cell carcinoma of the Cervix Uteri	AGA AGK ANXA5 CALR CANX CD109 CD44 CHPT1 DHDDS EPHX2 FOLR1 HPSE IL18R1 ITPKC LGALS1 MSLN MUTYH OGG1 PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SELE SMUG1 ST3GAL1 ST3GAL3 ST3GAL4 ST6GAL1 TM7SF2 TP53 TYMP UGT1A1	10232 10855 135228 175 1890 2053 2348 23583 2923 308 3956 4595 4968 5290 5291 5293 5294 54658 55750 56994 5728 6401 6480 6482 6484 6487 7108 7157 79947 80271 811 821 8809 960	Homo sapiens (human)
DOID:0080523	adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Aliases: hereditary diffuse leukoencephalopathy with spheroids	CTSA	5476	Homo sapiens (human)
DOID:0080302	mixed sleep apnea Aliases: complex sleep apnea	ACE CYP1A2 CYP2J2 ENOSF1 GNE GNPTAB IDS LGALS3 NANS PTEN PTGS2	10020 1544 1573 1636 3423 3958 54187 55556 5728 5743 79158	Homo sapiens (human)
DOID:12145	detrusor sphincter dyssynergia	SIGLEC7	27036	Homo sapiens (human)
DOID:0080094	myofibrillar myopathy 3 Aliases: LGMD 1A autosomal dominant limb-girdle muscular dystrophy type 1A myotilinopathy spheroid body myopathy	ACE ACHE AGL APRT B3GALNT2 B4GALNT2 B4GAT1 CHKA CHKB CRPPA DAG1 DCN DPEP1 DPM1 DPM2 DPM3 ENO1 FKRP FKTN GK GLB1 GMPPB HPGDS IDH2 IMPA1 INPP5B INPP5K LARGE1 LARGE2 LGALS3 MBL2 MGAM PARP1 PIK3C2A PMM2 POGLUT1 POMGNT1 POMGNT2 POMK POMT1 POMT2 PRG2 RXYLT1 SDC2 SI SYNJ1 SYNJ2	10329 10585 11041 1119 1120 120071 124872 142 148789 1605 1634 1636 178 1800 2023 2218 2710 2720 27306 29925 29954 3418 353 3612 3633 3958 4153 43 51763 5286 5373 54344 5553 55624 56983 6383 6476 729920 79147 84197 84892 8813 8818 8867 8871 8972 9215	Homo sapiens (human)
DOID:13336	congenital toxoplasmosis Aliases: Toxoplasmosis - congen.	ALOX12 ENPP1	239 5167	Homo sapiens (human)
DOID:0110124	Bardet-Biedl syndrome 2 Aliases: BBS2	INPP5E PIGX	54965 56623	Homo sapiens (human)
DOID:9840	esotropia Aliases: Convergence in manifest squint Internal Strabismus crossed eyes	AGRN ALG9 B3GAT3 CHAT CHST3 CYB5R3 DDOST GBA1 GMPPB PGAP2 PGAP3 PIGL PIGN PIGO PIGT PIGV PIGW PIGY PMM2 SLC35A2	1103 1650 1727 23556 26229 2629 27315 284098 29925 375790 51604 5373 55650 7355 79796 84720 84992 93210 9469 9487	Homo sapiens (human)
DOID:14452	hypokalemic periodic paralysis Aliases: Hypokalemic familial periodic paralysis Periodic paralysis I Westphal disease familial hypokalemic periodic paralysis periodic hypokalemic paralysis	PRKAA2	5563	Homo sapiens (human)
DOID:0080177	hepatic veno-occlusive disease Aliases: veno-occlusive disease	CD22 FCN2 HPSE TYMP XYLT2	10855 1890 2220 64132 933	Homo sapiens (human)

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