GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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 **4051 - 4075** of **7942** in total

« First

‹ Prev

…

159

160

161

162

163

164

165

166

167

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:8536	herpes zoster Aliases: Shingles herpes zona	ARSA CYP11A1 CYP17A1 ENOSF1 GP2 TECTA TNF	1583 1586 2813 410 55556 7007 7124	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0111257	gamma-glutamyl transpeptidase deficiency Aliases: GGT deficiency GGT1 deficiency GTG deficiency gamma-glutamyl transferase deficiency glutathionuria	GGT1 PLOD3	2678 8985	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:5534	renal pelvis squamous cell carcinoma Aliases: Epidermoid carcinoma of the kidney Pelvis	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:6945	inverted follicular keratosis Aliases: Inverted folicular keratosis	CYP24A1 HK2 INPP5A LGALS3 MMUT NTHL1 PIK3CA PIK3CB PIK3CD PIK3CG PLD2 PPT1 PTGS2 SDHD	1591 3099 3632 3958 4594 4913 5290 5291 5293 5294 5338 5538 5743 6392	Homo sapiens (human)	DisGeNET DisGeNET
DOID:5660	lymphoepithelioma-like carcinoma Aliases: Nasopharyngeal type Undifferentiated carcinoma lymphoepithelial carcinoma	PIK3CA SMUG1	23583 5290	Homo sapiens (human)	DisGeNET
DOID:0050475	Weill-Marchesani syndrome Aliases: GEMSS syndrome Marchesani-Weill Syndrome Mesodermal Dysmorphodystrophy, Congenital Spherophakia Brachymorphia Syndrome congenital mesodermal dystrophy	CERS3 TNF	204219 7124	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:13133	HELLP syndrome	GAPDH HADHA HPGDS HSPG2 IL18R1 MBL2 SIRT4 SLC17A5	23409 2597 26503 27306 3030 3339 4153 8809	Homo sapiens (human)	DisGeNET
DOID:12466	secondary hyperparathyroidism	ALPL CYP24A1 CYP27B1 CYP2B6 CYP2R1 CYP3A4 KL PIK3CA PIK3CB PIK3CD PIK3CG PTGS2 UMOD	120227 1555 1576 1591 1594 249 5290 5291 5293 5294 5743 7369 9365	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:2855	hyperthyroxinemia	ADH5	128	Homo sapiens (human)	DisGeNET
DOID:2913	acute pancreatitis	ACE ADH1B ADH1C ADH4 ADH5 AGPAT2 AKR1A1 AKR1B10 ALDH2 AMT AMY2A BCKDHA BCKDHB CAT CD14 CD38 CEACAM5 CEL CPTP CYP1A1 CYP24A1 CYP2E1 DBT FCGR3B FUT2 G6PC1 GPIHBP1 HMGCL HPSE ICAM1 ISYNA1 KL LEP LGALS3 LPL MBL2 MMUT MTAP PCCA PCCB PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PLA2G7 PLAUR PNLIP PNLIPRP2 PTEN PTGS2 QTRT1 REG1B REG3G SELE SELL SFTPD SIRT2 SLC17A5 SLC37A4 SMUG1 SPHK2 ST8SIA4 SULF1 SULF2 TIGAR TM7SF2 UGT1A7 UMOD VCAM1	10327 1048 10555 1056 10855 125 126 127 128 130120 1543 1571 1591 1629 1636 217 2215 22933 23213 23583 2524 2538 2542 26503 275 279 3155 3383 338328 3952 3958 4023 4153 4507 4594 5095 5096 51477 5290 5291 5293 5294 5320 5329 5406 5408 54577 55959 56848 57016 57103 5728 5743 593 594 5968 6401 6402 6441 7108 7369 7412 7903 7941 80772 81890 847 929 9365 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:3892	insulinoma Aliases: Insulin-Producing tumor of Islet cells Islet cell adenoma	ABO ACO2 ACSS2 CAT CD44 CHGA DHCR24 ENPP1 G6PC1 G6PC2 GAD1 GAD2 GCK GPD2 HK1 INPPL1 INS KL LGALS3 MCAT MRC1 NCAM1 PCYT1A PDHX PIK3CG PKD1 PLA2G15 PTEN PYGM SDHA SDHB SDHD SLC2A2 SLC2A3 TKT TNKS	1113 1718 23659 2538 2571 2572 2645 27349 28 2820 3098 3630 3636 3958 4360 4684 50 5130 5167 5294 5310 55902 5728 57818 5837 6389 6390 6392 6514 6515 7086 8050 847 8658 9365 960	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:10113	trypanosomiasis	ABO ACAT1 ACE ACHE ALOX5 ALPI ALPP APRT CALR COLEC11 CS CYP21A2 CYP2B6 CYP51A1 DDOST DHCR24 FCN2 FDPS G6PD GAD1 GAPDH GCK GLUL LGALS3 LGALS9 LSS MASP2 MBL2 MICA MTAP NT5E PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLCB1 PLCB4 PNP PTGS2 RPIA SDC4 SIRT2 SMPD1 SMUG1 SOAT1 STS STT3A STT3B TPI1	100507436 10747 142 1431 1555 1589 1595 1636 1650 1718 201595 2220 2224 22933 22934 23236 23583 240 248 250 2539 2571 2597 2645 2752 28 353 3703 38 3958 3965 4047 412 4153 43 4507 4860 4907 5290 5291 5293 5294 5332 5743 6385 6609 6646 7167 78989 811	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0110173	Charcot-Marie-Tooth disease axonal type 2U Aliases: CMT2U Charcot-Marie-Tooth neuropathy type 2U autosomal dominant Charcot-Marie-Tooth disease type 2U autosomal dominant axonal Charcot-Marie-Tooth disease type 2U	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:5296	liver leiomyosarcoma Aliases: leiomyosarcoma of the Liver	SMUG1	23583	Homo sapiens (human)	DisGeNET
DOID:0110479	autosomal recessive nonsyndromic deafness 21 Aliases: DFNB21 autosomal recessive deafness 21	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 DisGeNET Alliance of Genome Resources
DOID:13378	Kawasaki disease Aliases: Kawasaki's disease MLNS acute febrile MCLS acute febrile mucocutaneous lymph node syndrome mucocutaneous lymph node syndrome	ABO ACE ACHE ADIPOQ AMACR ATP6AP2 CAT CD14 CD177 CD209 CEACAM5 CERS6 CHI3L1 CLEC6A CLEC7A CYP2C9 CYP2E1 FCER2 FCGR3B FCN1 FUT1 GAPDH GLB1 HSD11B2 ICAM1 IL1R1 IL1RAP ITPKC KLRC1 KLRK1 LDHA MBL2 MDGA1 NCAM1 OLR1 PGK1 PLA2G7 PLCB1 PLCB4 PTGS2 SDC1 SELE SELP SLC35F5 ST6GAL1 STS TLR4 TNF ULBP1 VCAM1	10159 1048 1116 1559 1571 1636 2208 2215 2219 22914 23236 23600 2523 253782 2597 266727 2720 28 30835 3291 3383 3554 3556 3821 3939 412 4153 43 4684 4973 5230 5332 57126 5743 6382 6401 6403 64581 6480 7099 7124 7412 7941 80255 80271 80329 847 929 9370 93978	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0110499	autosomal recessive nonsyndromic deafness 40 Aliases: DFNB40 autosomal recessive deafness 40	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:0060643	primary sclerosing cholangitis	AGA ARSA B3GAT1 CD14 CEACAM5 CEACAM7 CLEC16A DLAT FUT2 FUT3 GAL3ST2 ICAM1 IL18R1 IL1R1 INPP5A KLRK1 LSS MANBA MGLL MICA NCAM1 NEIL1 PIK3CD PLA2G10 PLA2G2A PLA2G2D PNPLA3 PTGES PTGS2 SDC1 SLC17A5 SMUG1 STS TNF	100507436 1048 1087 11343 1737 175 22914 23274 23583 2524 2525 26279 26503 27087 3383 3554 3632 4047 410 412 4126 4684 5293 5320 5743 6382 64090 7124 79661 80339 8399 8809 929 9536	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:12801	mucopolysaccharidosis III Aliases: Mucopolysaccharidosis, MPS-III N-sulphoglucosamine sulphohydrolase deficiency Sanfilippo's syndrome heparan sulfate sulfatase deficiency	ACAN AGA APRT ARSA ARSB ARSG ARSH CANX CAT CD1D CD38 CHAT CTSA DPEP1 EXT1 EXT2 EXTL2 EXTL3 FUCA1 FUT1 GALNS GLB1 GNE GNPTAB GNPTG GNS GUSB HGSNAT HYAL1 HYAL2 IDS IDUA L1CAM MAN2B1 NAGLU NAGPA NEU1 NT5E OGA SGSH SLC26A2 SLC35G1 SPAM1 SUMF1	10020 10724 1103 138050 159371 175 176 1800 1836 2131 2132 2135 2137 22901 2517 2523 2588 2720 2799 285362 2990 3373 3423 3425 347527 353 3897 410 411 4125 4669 4758 4907 51172 5476 6448 6677 79158 821 84572 847 8692 912 952	Homo sapiens (human)	Glyco-Disease Genes Database Glyco-Disease Genes Database DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060190	ileocolitis	ACAT1 ACE ACSBG1 ALOX12 ALOX15 ALOX5 ALPL ANXA5 ARSA ASAH1 B4GALT7 CALR CAT CD14 CD177 CD1D CD44 CD55 CEACAM5 CEACAM6 CERK CERS2 CERS6 CH25H CHGA CHI3L1 CHST15 CHST4 CLEC7A CNTN3 CPT1B CRLS1 CSPG4 CTSA CYP27B1 CYP7B1 EFNA5 ENPP2 FDPS FUT2 FUT3 G6PC3 GALM GPIHBP1 GPX1 GPX2 GUSB HACD1 HPGDS HPRT1 HYAL2 ICAM1 IDH2 IL18R1 IL1R1 IL1RAP IL1RL2 INPP5D ISYNA1 KL LAYN LCT LGALS1 LGALS2 LGALS3 LPIN1 LYZ MBL2 MRC1 NAMPT NT5E OGA PARP1 PC PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G10 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLB1 PLCG1 PLD1 PLD2 PRKAA2 PRSS8 PSAP PSMD10 PTEN PTGDS PTGES PTGS1 PTGS2 REG3G RGN SDC1 SDC2 SDC4 SELL SELP SFTPD SGMS2 SGPL1 SGPP1 SGPP2 SI SIGLEC1 SIGLEC8 SIRT6 SLC33A1 SMPD1 SMUG1 SPHK1 ST8SIA2 STS TM7SF2 VCAM1 VNN1 VTCN1	10135 10164 1048 10724 1113 1116 11285 130120 130367 130589 1375 142 143903 1464 151056 1594 1604 1636 166929 1946 2224 23175 23205 23583 239 240 246 249 2524 2525 253782 27181 27306 2876 2877 2990 29956 308 3251 3383 338328 3418 3554 3556 3635 38 3938 3956 3957 3958 4069 410 412 4153 427 4360 4680 4907 5067 5091 51363 51477 51548 5168 5290 5291 5293 5294 5315 5319 5320 5321 5335 5337 5338 54675 5476 5563 5652 5660 57126 5716 5728 5730 5742 5743 6382 6383 6385 6402 6403 6441 64581 6476 64781 6609 6614 7108 7412 79679 811 8128 81537 8398 8399 847 8692 8808 8809 8876 8877 8879 9023 9104 912 9197 9200 92579 929 9365 9420 9536 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:1580	diffuse scleroderma Aliases: diffuse systemic sclerosis systemic sclerosis, diffuse	ADIPOQ CAT HEXA PTEN TLR2	3073 5728 7097 847 9370	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:5381	bile duct adenoma Aliases: Cholangioadenoma	BRAF NCAM1	4684 673	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0050540	Charcot-Marie-Tooth disease type 3 Aliases: DEJERINE-SOTTAS NEUROPATHY DEJERINE-SOTTAS SYNDROME	AMACR CAT CYP4F3 FIG4 GPX2 HPSE LPIN1 MTMR2 PLCB4 PLCE1 PTGS2	10855 23175 23600 2877 4051 51196 5332 5743 847 8898 9896	Homo sapiens (human)	DisGeNET
DOID:13884	sick sinus syndrome Aliases: sinus node infection	ACADM ACE ACOT7 ALDH2 ALG10 ALG10B APRT CACNA2D1 CACNA2D2 CALR CAT CD38 CHI3L1 CHPT1 CPT1A CPT2 CYP19A1 EPHX2 GLA GPC3 GPD1L GYG1 HACD1 HADHA HADHB HJV HSPG2 ICAM1 IDS ITPKB LGALS3 PCCA PCCB PCYT1A PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PLB1 PRKAA2 PTGS2 SCD SELP SIGLEC7 SLC33A1 SMUG1 SQLE UGCG VCAM1	1116 11332 1374 1376 144245 148738 151056 1588 1636 2053 217 23171 23583 27036 2717 2719 2992 3030 3032 3339 3383 34 3423 353 3707 3958 5095 5096 5130 5236 5290 5291 5293 5294 5563 56994 5743 6319 6403 6713 7357 7412 781 811 847 84920 9197 9200 9254 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:9503	Loeffler syndrome Aliases: Loeffler's pneumonia Loffler's syndrome	ALPL CEL CHI3L1 HPGDS IL1R1 IL1RL1 ISYNA1 PARP9 PTGDS SIGLEC8 SIRT2 SLC27A5	1056 10998 1116 22933 249 27181 27306 3554 51477 5730 83666 9173	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements