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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 **2576 - 2600** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:12120	pulmonary alveolar proteinosis	CEACAM5 CEL CHI3L1 CYP27A1 ENO2 PARP9 SFTPA1 SFTPC SFTPD SLC27A5 SOAT1	1048 1056 10998 1116 1593 2026 6440 6441 653509 6646 83666	Homo sapiens (human)
DOID:3908	lung non-small cell carcinoma Aliases: NSCLC Non-small cell lung cancer non-small cell lung carcinoma	ACACA ACE ACHE ACLY ACOT8 ACSS1 ACSS2 ADH1A ADH1B ADH1C ADH7 AGL AKR1A1 AKR1B10 AKR1C1 AKR1C2 AKR1C3 AKT1 ALDH1A3 ALDH1B1 ALDH3A1 ALDH3A2 ALDH7A1 ALG13 ALG1 ALOX15B ALOX5 AMACR ANXA4 ANXA5 APRT ARSF ATRNL1 B3GALNT1 B3GAT1 B3GNT3 BAAT BAD CA4 CACNA2D2 CALR CAT CBR1 CD14 CD177 CD1D CD33 CD38 CD44 CD55 CD74 CD93 CDH13 CEACAM5 CEACAM7 CEMIP CERS6 CHGA CHI3L1 CHKA CHODL CHPT1 CNTN1 CNTN2 COMT CRLS1 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP2E1 CYP2R1 CYP3A4 CYP3A5 CYP4F3 DCN DHCR24 DHDDS DHDH EFNA1 ENO1 ENO2 EXTL3 FASN FBP1 FBXO17 FCGR3B FH FOLR2 FUT4 FUT8 G6PD GALC GALNS GALNT14 GAPDH GCNT3 GFPT2 GLDC GLUL GML GOLPH3 GPC3 GPC5 GPX1 GPX3 HAGH HAS2 HAS3 HK1 HK2 HMMR HPGDS HPRT1 HPSE HS3ST2 HS3ST3B1 HSD11B2 HSD17B1 HSD17B6 HYAL1 ICAM1 IDH1 IDH2 IGF2R IL18R1 INPP4A INPP5D INPPL1 KAT2A KHK KL KLB KLRB1 KLRD1 KLRK1 L1CAM LDHA LDHB LDHC LEP LGALS1 LGALS3 LGALS9 LIPC LPCAT1 LPIN3 LPL LY6K LYPD3 LYPD5 LYPLA1 MBD4 MBL2 MCAT MDH1 MDH2 ME1 ME2 MICA MMUT MPG MRC1 MSLN MTAP MUTYH NAMPT NCAM1 NEIL1 NEU1 NEU3 NT5E NTHL1 OGG1 OPCML PAFAH1B1 PAPSS1 PARP1 PC PCK2 PDIA3 PFKFB3 PGAM1 PGK1 PIK3C2B PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKM PLA2G10 PLA2G2A PLA2G4A PLA2G6 PLAUR PLB1 PLCB3 PLCB4 PLCE1 PLCG1 PLCH1 POGLUT1 PPT1 PRG2 PRKAA1 PRKAA2 PRSS8 PSMD10 PTEN PTGES3 PTGES PTGIS PTGS1 PTGS2 PYGB RECK RGMB RGN RPN2 RTN4R SCD SDC4 SDHA SDHC SELE SFTPA1 SFTPA2 SFTPC SFTPD SGMS1 SHMT2 SIGLEC9 SIRT2 SIRT4 SIRT6 SLC17A5 SLC26A2 SLC2A3 SLC2A5 SLC3A2 SLC5A1 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 SRGN ST6GAL1 ST8SIA2 STS SULF2 TIGAR TM7SF2 TMTC3 TNF TNFRSF10C TNKS2 TNKS TP53 TREH TUSC3 TYMP UGCG UGP2 UGT1A1 UGT1A7 UGT1A9 ULBP1 UMPS UNG VCAM1 VTCN1 XXYLT1	10005 100507436 1012 10135 10232 10327 10331 10434 1048 10728 10825 10855 1087 1113 1116 11181 1119 115290 120227 124 125 126 1272 131 1312 140578 142 151056 152002 152831 1543 1544 1545 1555 1557 1558 1559 1571 1576 1577 1586 1588 1591 1593 1594 1604 160418 1634 1636 1645 1646 1718 178 1836 1890 1942 2023 2026 207 2137 218 219 2194 220 2203 2215 224 2262 2271 22914 22918 22933 23007 23409 2350 23583 23600 240 247 2526 2530 253782 2539 2581 2588 259230 2597 26033 2648 26503 27076 27087 27180 2719 27294 27306 2731 27349 2752 2765 284348 285704 2876 2878 2923 3029 3037 3038 307 308 3098 3099 31 3161 3251 3291 3292 3373 3383 3417 3418 3482 353 3631 3635 3636 3795 3820 3824 3897 3939 3945 3948 3952 3956 3958 3965 3990 4023 4051 412 4153 416 4190 4191 4199 4200 43 4350 4360 4507 4594 4595 4684 47 4758 4907 4913 4968 4978 501 5048 5091 5106 51196 51548 5209 5223 5230 5287 5289 5290 5291 5293 5294 5310 5315 5320 5321 5329 5331 5332 5335 54577 54600 54658 54675 54742 5538 5552 5553 5562 5563 55902 55959 56052 5652 56848 56983 56994 570 57016 57103 57126 5716 572 57214 5728 5740 5742 5743 5834 6185 6319 6385 6389 6391 6401 64083 6440 6441 6472 6480 64900 65078 6515 6518 6520 6523 653509 6609 6646 6900 7108 7124 7157 729238 7357 7360 7372 7374 7412 762 79623 79661 79679 79868 79888 7991 79947 80329 80351 811 8128 8398 8399 8434 84532 847 8630 8644 8658 8706 873 8794 8809 8877 8930 9061 9104 912 9245 9254 929 9365 945 952 9536 960 972 9945 9953 9956	Homo sapiens (human)
DOID:0050699	Dent disease Aliases: Dent disease 1 Dent disease 2 Dent's disease	CLC EXT2 INPP5B NAGLU OCRL	1178 2132 3633 4669 4952	Homo sapiens (human)
DOID:12387	nephrogenic diabetes insipidus	ATP6AP2 CANX G6PD L1CAM PRKAA2 PTGS2	10159 2539 3897 5563 5743 821	Homo sapiens (human)
DOID:9042	polyp of corpus uteri Aliases: endometrial/uterine polyp polyp of Endometrium polyp of the Uterus polyp, uterus	CYP19A1 PTEN PTGS2 SDC1	1588 5728 5743 6382	Homo sapiens (human)
DOID:0060258	reticulate acropigmentation of Kitamura Aliases: RAPK	ACAN COL9A2 COMT POFUT1 POGLUT1	1298 1312 176 23509 56983	Homo sapiens (human)
DOID:0110251	cataract 15 multiple types Aliases: CTRCT15	AGK ALDH7A1 CRYL1 CYP27A1 GALK1 GCNT2 GPC5 INPP5K LSS OCRL PTEN SLC33A1 SORD	1593 2262 2584 2651 4047 4952 501 51084 51763 55750 5728 6652 9197	Homo sapiens (human)
DOID:0110110	atrial heart septal defect 5 Aliases: ASD5 atrial septal defect 5	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:0060468	Holt-Oram syndrome Aliases: atrio-digital syndrome atriodigital dysplasia heart-hand syndrome	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:9673	ulcerative stomatitis	CAT FCGR3B MICA PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PPT1 PSAP UGT1A1 UNG	100507436 142 2215 5290 5291 5293 5294 54658 5538 5660 7374 847	Homo sapiens (human)
DOID:0090024	split hand-foot malformation 1 with sensorineural hearing loss Aliases: SHFM1D congenital deafness with split hands and feet	ENOSF1 IL18R1 OGG1 PIK3CA	4968 5290 55556 8809	Homo sapiens (human)
DOID:2855	hyperthyroxinemia	ADH5	128	Homo sapiens (human)
DOID:10632	Wolfram syndrome Aliases: WFS	COMT	1312	Homo sapiens (human)
DOID:2789	parasitic protozoa infectious disease Aliases: mastigophora infectious disease sarcomastigophora infectious disease	CYP51A1 HK1	1595 3098	Homo sapiens (human)
DOID:3306	mixed germ cell cancer Aliases: mixed germ cell neoplasm mixed germ cell tumor mixed germ cell tumour mixed teratoma and seminoma	CYP17A1	1586	Homo sapiens (human)
DOID:0060357	chylomicron retention disease Aliases: Anderson disease CMRD	AGA AMT ARSA ARSB ASAH1 CHIT1 CTSA CYP27A1 DGAT1 FADS2 G6PC1 G6PD GAA GALC GBA1 GBE1 GDPD3 GLA GLB1 GNPTAB GNPTG GPIHBP1 GUSB ICAM1 IDS IDUA LCAT LGALS3 LPL LSS MANBA MGAM NAGA NAGPA NT5E OGA PNPLA2 PTGDS SCD SELE SFTPD SI SLC2A3 SMPD1 SMUG1 UGCG UGT1A1 UMOD VCAM1	10724 1118 1593 175 23583 2538 2539 2548 2581 2629 2632 2717 2720 275 2990 3383 338328 3423 3425 3931 3958 4023 4047 410 411 4126 427 4668 4907 51172 54658 5476 57104 5730 6319 6401 6441 6476 6515 6609 7357 7369 7412 79153 79158 84572 8694 8972 9415	Homo sapiens (human)
DOID:0080821	exercise-induced bronchoconstriction Aliases: exercise-induced asthma	ALOX5	240	Homo sapiens (human)
DOID:0110704	hypotrichosis 7 Aliases: Hypt7 Lah2 hypotrichosis, localized, autosomal recessive 2 total Mari type hypotrichosis,	GLB1 PTGS2	2720 5743	Homo sapiens (human)
DOID:0110969	brachydactyly type B1 Aliases: BDB1	PARP1	142	Homo sapiens (human)
DOID:1928	Williams-Beuren syndrome Aliases: Fanconi Schlesinger syndrome WBS	ARSD CACNA2D1	414 781	Homo sapiens (human)
DOID:2640	struma ovarii	SMUG1	23583	Homo sapiens (human)
DOID:0110064	amelogenesis imperfecta type 1H Aliases: AI1H amelogenesis imperfecta type IH	AKR1C1 AKR1C2 MMP25 TMEM165	1645 1646 55858 64386	Homo sapiens (human)
DOID:0110227	cataract 32 multiple types Aliases: CTRCT32	ACE AGK ALDH7A1 CHI3L1 CRYL1 CYP1A1 CYP27A1 FCGR3B FCN2 GALK1 GCNT2 GPC5 INPP5K LSS MBL2 OCRL PTEN SDC4 SFTPA1 SFTPA2 SFTPD SLC17A5 SLC2A10 SLC33A1 SMC3 SMPD1 SORD	1116 1543 1593 1636 2215 2220 2262 2584 26503 2651 4047 4153 4952 501 51084 51763 55750 5728 6385 6441 653509 6609 6652 729238 81031 9126 9197	Homo sapiens (human)
DOID:11175	enophthalmos	ACHE ALG1 ALG9 ALPL B3GALT6 B4GALT7 COG4 EFNA5 FIG4 HAS2 ICAM1 PTEN SMUG1 UGDH XYLT1	11285 126792 1946 23583 249 25839 3037 3383 43 56052 5728 64131 7358 79796 9896	Homo sapiens (human)
DOID:0050431	arrhythmogenic right ventricular cardiomyopathy Aliases: ARVC ARVC cardiomyopathy ARVD arrhythmogenic right ventricular dysplasia arrhythmogenic right ventricular dysplasia/cardiomyopathy right ventricular ACM	FASN GNPTAB HACD1 IL18R1 PIK3CA PIK3CB PIK3CD PIK3CG	2194 5290 5291 5293 5294 79158 8809 9200	Homo sapiens (human)

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