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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 **1401 - 1425** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:9655	oral mucosa leukoplakia	ALDH2 CYP1A1 CYP1B1 CYP2E1 HPGDS LGALS1 LYZ OGG1 PTGS2 TP53	1543 1545 1571 217 27306 3956 4069 4968 5743 7157	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:13214	hole retinal cyst Aliases: Macular cyst or hole Macular cyst, hole, or pseudohole of retina Macular pseudohole retinal cyst	GALNS RPE	2588 6120	Homo sapiens (human)	DisGeNET
DOID:4163	ganglioneuroblastoma	CD44 GAPDH LGALS3 NCAM1 SIGLEC7	2597 27036 3958 4684 960	Homo sapiens (human)	DisGeNET
DOID:5518	penis squamous cell carcinoma Aliases: Epidermoid cell carcinoma of penis	CD109 PIK3CA PIK3CB PIK3CD PIK3CG PTEN	135228 5290 5291 5293 5294 5728	Homo sapiens (human)	DisGeNET
DOID:0050864	non-arteritic anterior ischemic optic neuropathy Aliases: non-arteritic anterior ischaemic optic neuropathy nonarteritic anterior ischaemic optic neuropathy nonarteritic anterior ischemic optic neuropathy	ACE	1636	Homo sapiens (human)	Alliance of Genome Resources
DOID:5411	lung oat cell carcinoma Aliases: oat cell carcinoma	CBR1 CD44 CEACAM5 CHGA CYP1A1 CYP2E1 ENO2 LGALS3 MRC1 NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SMUG1 STS UGT1A1	1048 1113 1543 1571 2026 23583 3958 412 4360 4684 5290 5291 5293 5294 54658 5728 873 960	Homo sapiens (human)	DisGeNET
DOID:0050460	Wolf-Hirschhorn syndrome Aliases: 4p deletion syndrome PITT SYNDROME Pitt-Rogers-Danks Syndrome chromosome 4p16.3 deletion syndrome	IL1RL1	9173	Homo sapiens (human)	DisGeNET
DOID:8927	learning disability Aliases: Academic skill disorder learning disorder	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 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 KDSR KL L1CAM L2HGDH LARGE1 LDHA LDHD LFNG LSS MACROD2 MAG MAN1B1 MAN2B1 MAN2C1 MANBA MASP1 MBOAT7 MMUT NAGA NAGLU NANS NDST1 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 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 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 85365 8733 8794 8802 8867 8869 90161 9060 9091 9126 9197 9200 9215 92579 93210 9365 9487 9488 952 9524 9651 9791 9993	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:8955	sideroblastic anemia Aliases: ANEMIA SIDEROBLASTIC Anemia, hypochromic with iron loading	CALR CYP2E1	1571 811	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0080483	peroxisome biogenesis disorder 8A Aliases: peroxisome biogenesis disorder 8A (Zellweger)	CAT G6PD	2539 847	Homo sapiens (human)	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:0080073	spina bifida occulta	B3GLCT COLEC10 COLEC11 LFNG MASP1	10584 145173 3955 5648 78989	Homo sapiens (human)	DisGeNET
DOID:0080201	Peters plus syndrome Aliases: Krause-Kivlin syndrome Peters anomaly-short limb dwarfism syndrome Peters-plus syndrome	B3GALT1 B3GLCT POFUT2	145173 23275 8708	Homo sapiens (human)	Glyco-Disease Genes Database DisGeNET Alliance of Genome Resources
DOID:9741	biliary tract disease	CD14 CYP3A4 LYZ PIK3CA PIK3CB PIK3CD PIK3CG PNPLA6 VCAM1	10908 1576 4069 5290 5291 5293 5294 7412 929	Homo sapiens (human)	DisGeNET
DOID:2615	papilloma Aliases: papillomatosis	ALDH3A2 AMACR ARSF B3GAT1 CALR CAT CEACAM5 DCN EBP GLB1 GOLPH3 ICAM1 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PLA2G4A PTEN PTGES PTGS2 SDC1 SDHB SDHC SDHD ST8SIA4 STS TM7SF2 XYLT2	1048 10682 1634 224 23600 27087 2720 3383 412 416 5290 5291 5293 5294 5310 5321 5728 5743 6382 6390 6391 6392 64083 64132 7108 7903 811 847 9536	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2047	hepatitis D Aliases: delta hepatitis	B3GAT1 GAPDH SLC35A2 SOAT1 UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9	2597 27087 54575 54576 54577 54578 54579 54600 54657 54658 54659 56886 6646 7355	Homo sapiens (human)	DisGeNET
DOID:2452	thrombophilia Aliases: hypercoagulability state	A4GALT ABO ACE ACSM3 ACSS2 ALG6 ANXA5 B3GAT2 CALR CAT CD14 CEACAM5 CEACAM7 CHI3L1 CLEC1B COMT CYP19A1 CYP1A1 CYP1A2 CYP2C9 CYP3A5 CYP4F2 DLD DPM1 DPM2 EXT1 FCGR3B GBGT1 GFRA1 GLA GPI GPX3 HPSE IDH1 IDH2 LCT LPL LTC4S MBL2 MGAT2 MGLL MPI NGLY1 NT5E PC PIGA PIGM PLA2G15 PLA2G1B PLA2G2A PLA2G6 PLB1 PLCG2 PMM2 PPP1R3B PPP1R3C PTEN SCD SDC1 SELE SELP SMPD1 SMUG1 SRD5A3 ST3GAL4 STS TKTL1 TM7SF2 VCAM1	1048 10855 1087 1116 11343 1312 135152 151056 1543 1544 1559 1577 1588 1636 1738 2131 2215 23583 23659 26301 2674 2717 28 2821 2878 29929 308 3417 3418 3938 4023 4056 412 4153 4247 4351 4907 5091 51266 5277 5319 5320 5336 5373 53947 5507 55768 55902 5728 6296 6319 6382 6401 6403 6484 6609 7108 7412 79644 79660 811 8277 8398 847 8529 8813 8818 929 93183	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET 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:0070216	familial hyperinsulinemic hypoglycemia 3 Aliases: HHF3 hyperinsulinemic hypoglycemia due to glucokinase deficiency hyperinsulinism due to glucokinase deficiency	GCK	2645	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:13364	obsolete chronobiology disease	ACE	1636	Homo sapiens (human)	DisGeNET
DOID:0080502	GM1 gangliosidosis type 1	ARSA CHIT1 CTSA CYP2U1 GLB1 NEU1	1118 113612 2720 410 4758 5476	Homo sapiens (human)	Glyco-Disease Genes Database DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060183	collagenous colitis	CHGA PTEN	1113 5728	Homo sapiens (human)	DisGeNET
DOID:7147	ankylosing spondylitis Aliases: Bekhterev syndrome Bekhterev's disease Marie-Strumpell disease	ACE ADIPOQ ALPL ALPP ARSA ATRNL1 CAT CD14 CD38 CD74 CLEC16A CYP1A1 CYP1B1 CYP24A1 CYP2C9 CYP3A5 DAG1 DLAT DPEP1 ENPP1 FCGR3B FUT2 GAL3ST2 IL18R1 IL1R1 LGALS3 LSS MBL2 MICA NT5E PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGIS PTGS2 SCD5 SELP SFTPA2 SGSH SIGLEC7 SOAT1 ST8SIA4 SULT1E1 TLR4 UGT2B17 UST	100507436 10090 1543 1545 1559 1577 1591 1605 1636 1737 1800 2215 23274 249 250 2524 26033 27036 3554 3958 4047 410 4153 4907 5167 5290 5291 5293 5294 5728 5740 5743 6403 64090 6448 6646 6783 7099 729238 7367 7903 79966 847 8809 929 9370 952 972	Homo sapiens (human)	DisGeNET Alliance of Genome Resources

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