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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 **1876 - 1900** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:1085	Edwards syndrome Aliases: Complete trisomy 18 syndrome E3 Trisomy trisomy 18	CD38 FUT1	2523 952	Homo sapiens (human)	DisGeNET DisGeNET
DOID:4440	seminoma Aliases: Seminoma, Pure	ACACA ACE ALDH1A3 ALDH7A1 ALOX12B ALOX5 ALPP CD44 CLGN CYP17A1 CYP19A1 CYP1A1 CYP2B6 CYP3A5 CYP3A7 ETNK1 GCNT1 GGT1 GPC3 HMMR HPGDS HSD17B4 ICAM1 IL18R1 KCNQ1 L1CAM LDHC LGALS3 LY6K MCFD2 MRC1 PCNA PCYT1A PGD PIK3CA PIK3CB PIK3CD PIK3CG PLAAT3 PSMD10 PTEN SLC2A5 SMUG1 SPACA3 STS SULF1 SULF2 TKTL1 TYMP UGT1A1	1047 11145 124912 1543 1551 1555 1577 1586 1588 1636 1890 220 23213 23583 240 242 250 2650 2678 2719 27306 31 3161 3295 3383 3784 3897 3948 3958 412 4360 501 5111 5130 5226 5290 5291 5293 5294 54658 54742 55500 55959 5716 5728 6518 8277 8809 90411 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:7188	autoimmune thyroiditis Aliases: Chronic Lymphocytic Thyroiditis Hashimoto thyroiditis Hashimoto's Disease Hashimoto's syndrome Hashimoto's thyroiditis Lymphocytic Thyroiditis	CD14 CD38 CYP19A1 CYP21A2 CYP27B1 DAG1 FUT2 GAD1 GAD2 GLUL GPX3 ICAM1 IL18R1 IL18RAP IL1RL1 LGALS3 MBL2 NCAM1 NT5E PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLCG2 PTEN PTGDS PTGS2 RENBP SOAT1	1588 1589 1594 1605 2524 2571 2572 2752 2878 3383 3958 4153 4684 4907 5130 5290 5291 5293 5294 5336 5728 5730 5743 5973 6646 8807 8809 9173 929 952	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060402	chromosome 17p13.1 deletion syndrome	ALPP ATRNL1 CD33 CD38 COMT CYP2B6 FCN2 OCRL PAFAH1B1 PIGA PIGN PLCB1 PLCE1 PLCG1 PTEN SLC17A5	1312 1555 2220 23236 23556 250 26033 26503 4952 5048 51196 5277 5335 5728 945 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B Aliases: CMTDI1 CMTDIB Charcot-Marie-Tooth neuropathy dominant intermediate B DI-CMTB	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)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:14654	prostatitis	CYP19A1 HADHA HADHB PTGS2 SMUG1	1588 23583 3030 3032 5743	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:4554	type C thymoma Aliases: Thymoma, type C	CD74 HACD1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGES2 PTGES PTGS2 SMUG1	23583 5290 5291 5293 5294 5728 5743 80142 9200 9536 972	Homo sapiens (human)	DisGeNET
DOID:0110540	autosomal recessive nonsyndromic deafness 98 Aliases: DFNB98 autosomal recessive deafness 98	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:14484	sporotrichosis	ABO ATP6V1A CAT CD14 CD209 CLEC1A CLEC7A CYP2C19 CYP51A1 LGALS1 MASP2 MBL2 MRC1	10747 1557 1595 28 30835 3956 4153 4360 51267 523 64581 847 929	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:14271	acute cholangitis	CAT	847	Homo sapiens (human)	DisGeNET
DOID:0080325	tuberous sclerosis 2	NTHL1 PKD1 PTEN	4913 5310 5728	Homo sapiens (human)	DisGeNET
DOID:9538	multiple myeloma Aliases: myeloma	ABO ACE ACSBG1 ALOX5 ALPI ALPP AMY1A AMY1B AMY1C ANXA5 APRT B3GAT1 BST2 CANX CAT CD14 CD1D CD22 CD33 CD38 CD44 CD48 CD74 CEACAM6 CHI3L1 CHPT1 CLEC12A COLEC10 CPT1C CRYBG1 CYP1A1 CYP1B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP3A4 DCN DHCR24 DHDDS DLD ENO1 ENPP1 ENPP2 EXT1 FASN FCER2 FCGR3B FDPS FH FOLR1 FOLR2 FUT1 G6PD GAPDH GBA1 GLB1 GLO1 GPX1 GPX3 HAS1 HAS2 HK1 HK2 HMMR HPGDS HPSE2 HPSE ICAM1 IDH1 IDH2 IDUA IGF2R IL1RL1 INPP5D INPPL1 KL KLRB1 KLRC1 KLRK1 LDHA LGALS1 LGALS3 LGALS4 LGALS8 LGALS9 LPL MBL2 MCAT MICA MINPP1 MMP25 MPG MRC1 NAGLU NAMPT NCAM1 NEIL1 OGA PAFAH1B1 PARP14 PARP1 PCYT1A PFKFB3 PIGA PIK3CA PIK3CB PIK3CD PIK3CG PIKFYVE PKM PLAUR PPT2 PRKAA2 PSAP PSMD10 PTEN PTGS1 PTGS2 RECK RENBP RPIA SDC1 SELE SELL SELP SIGLEC1 SIRT6 SLC2A12 SLC2A4 SLC2A8 SLC35A4 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 SRGN ST3GAL6 TDG TNF TNFRSF10C TNKS TP53 TYMP UGCG ULBP2 VCAM1 VCAN	100507436 10135 10402 10584 10724 10855 1116 113829 126129 142 1462 154091 1543 1545 1555 1557 1558 1559 1576 160364 1634 1636 1718 1738 1890 200576 202 2023 2131 2194 2208 2215 2224 2271 22914 22934 23205 2348 2350 23583 240 248 250 2523 2539 2597 2629 27087 2720 27306 27349 2739 276 277 278 28 2876 2878 29988 3036 3037 308 3098 3099 3161 3383 3417 3418 3425 3482 353 3635 3636 3820 3821 3939 3956 3958 3960 3964 3965 4023 4153 4350 4360 4669 4680 4684 5048 5130 51548 5167 5168 5209 5277 5290 5291 5293 5294 5315 5329 54625 5552 5563 5660 56848 56994 5716 5728 5742 5743 5973 60495 6382 6401 6402 6403 64386 6517 6609 6614 6646 684 6996 7124 7157 7357 7412 79661 79947 80328 821 8434 847 8658 8794 8877 912 9173 929 933 9365 9374 945 952 9562 960 962 972	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:12918	thromboangiitis obliterans Aliases: Buerger's disease Presenile gangrene	CD14 CD44 HPSE ICAM1 LGALS9 MICA PIK3CA PIK3CB PIK3CD PIK3CG PTGS2 SELE SMC3 SPAM1 ST3GAL5 ST8SIA1 VCAM1	100507436 10855 3383 3965 5290 5291 5293 5294 5743 6401 6489 6677 7412 8869 9126 929 960	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:7061	obsolete precursor B lymphoblastic lymphoma/leukemia	PARP1	142	Homo sapiens (human)	DisGeNET
DOID:0060253	scapuloperoneal myopathy	ALOX5	240	Homo sapiens (human)	DisGeNET
DOID:0090044	dystonia 9	SLC2A1	6513	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090100	ocular albinism with sensorineural deafness Aliases: WS2-OA autosomal recessive Waardenburg syndrome type 2 with ocular albinism digenic Waardenburg syndrome/albinism digenic Waardenburg syndrome/ocular albinism	IDS	3423	Homo sapiens (human)	DisGeNET
DOID:12365	malaria Aliases: induced malaria	ABO ACACA ACE ACHE ACOT7 ADH1B AKR1A1 ALOX5 ANXA4 ANXA7 B3GAT1 CAT CD14 CD1D CD55 CDH13 CEL CERS1 CFC1 CHI3L1 CHIT1 CS CYP1A2 CYP2B6 CYP2C19 CYP2C8 CYP3A4 ENO2 ENOSF1 FCGR3B FCN2 FUT9 G6PD GAPDH GLO1 GOLPH3 GPX1 H6PD HK1 HPGDS HPRT1 HPSE HSD11B1 ICAM1 IL18R1 IL1R1 ISYNA1 LMAN1 MASP2 MBL2 MCAT MOGS MPPE1 NANP PGAM1 PGD PGLS PGM1 PKLR PNP POFUT2 POMGNT2 PSAP PTGS2 SDC1 SELE SPHK1 TMED9 TNF UMPS VNN1 VNN2	1012 10327 1056 10690 10715 10747 10855 1116 1118 11332 125 140838 1431 1544 1555 1557 1558 1576 1604 1636 2026 2215 2220 23275 240 2539 25796 2597 27087 27306 27349 2739 28 2876 307 3098 31 310 3251 3290 3383 3554 3998 4153 43 4860 51477 5223 5226 5236 5313 54732 55556 55997 5660 5743 6382 6401 64083 65258 7124 7372 7841 847 84892 8809 8875 8876 8877 912 929 9563	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0060452	posterior amorphous corneal dystrophy Aliases: PACD chromosome 12q21.33 deletion syndrome	DCN	1634	Homo sapiens (human)	DisGeNET
DOID:3112	papillary adenocarcinoma Aliases: Infiltrating and papillary adenocarcinoma infiltrating papillary adenocarcinoma	ACE ACHE AGK AGRN AKR1C2 ALDH1A3 ALOX12B ALOX5 AMACR ANXA4 ANXA5 APRT B4GALNT3 CD38 CD44 CD74 CEMIP CERS1 CERS2 CHI3L1 CPT1C CYP19A1 CYP1A1 CYP24A1 CYP27B1 CYP2R1 DCN DHCR24 EBP ELOVL2 ENPP2 FASN FCER2 FCGR3B FH FUCA1 FUT4 G6PD GAPDH GAS1 GGT1 GLA GPC3 GPI GPNMB GPX3 GUSB HK2 HPGDS HPRT1 HPSE ICAM1 IDH1 IL1R1 INPP4B INPPL1 KLB L1CAM LDHA LDHB LGALS1 LGALS3 LMAN2L MCAT MINPP1 MMUT MRC1 NCAM1 NT5E OGG1 PARG PARP1 PC PCYT1A PDHB PGK1 PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G1B PLA2G2A PLA2G6 PLD2 PRKAA2 PTEN PTGDS PTGES3 PTGES PTGIS PTGS2 RECK RPIA SCD SDC4 SDHB SELE SELL SHMT1 SIRT6 SLC2A3 SMUG1 SPHK1 SPHK2 TKTL1 TM7SF2 TPI1 TYMP UGCG	10457 10682 10715 10728 10855 1116 120227 126129 142 152831 1543 1588 1591 1594 1634 1636 1646 1718 1890 2194 220 2208 2215 2271 22934 23583 23600 240 242 2517 2526 2539 2597 2619 2678 2717 2719 27306 27349 2821 283358 2878 2990 29956 307 308 3099 3251 3383 3417 353 3554 3636 375790 3897 3939 3945 3956 3958 43 4360 4594 4684 4907 4968 5091 5130 51548 5162 5168 5230 5236 5290 5291 5293 5294 5315 5319 5320 5338 54898 5563 55750 56848 57214 5728 5730 5740 5743 6319 6385 6390 6401 6402 6470 6515 7108 7167 7357 81562 8277 8398 8434 8505 8821 8877 952 9536 9562 960 972	Homo sapiens (human)	DisGeNET DisGeNET
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)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0050437	Danon disease Aliases: ANTOPOL DISEASE PSEUDOGLYCOGENOSIS II	APRT	353	Homo sapiens (human)	DisGeNET
DOID:0080347	malignant pheochromocytoma Aliases: Pheochromocytoma, malignant	SDHB	6390	Homo sapiens (human)	DisGeNET
DOID:3275	thymoma	CAT CD44 CD74 CLEC14A G6PD GAPDH GPX1 HACD1 HSD17B7 ICAM1 LY75 MICA MSLN PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTEN PTGES2 PTGES PTGS2 SMUG1 SULT1E1	100507436 10232 142 161198 23583 2539 2597 2876 3383 4065 51478 5290 5291 5293 5294 5716 5728 5743 6783 80142 847 9200 9536 960 972	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0050747	obsolete lymphoplasmacytic lymphoma	ACADVL ACSBG1 ANXA5 CD22 CD38 CD55 CLEC12A COLEC10 FCER2 HAS1 HAS2 HMMR LIPC LPL NAMPT NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PLCG2 SLC35B2 SMUG1 SOAT1	10135 10584 160364 1604 2208 23205 23583 3036 3037 308 3161 347734 37 3990 4023 4684 5290 5291 5293 5294 5336 6646 933 952	Homo sapiens (human)	DisGeNET DisGeNET

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