GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

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 **3626 - 3650** of **7942** in total

« First

‹ Prev

…

142

143

144

145

146

147

148

149

150

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲
DOID:234	colon adenocarcinoma Aliases: Colonic adenocarcinoma adenocarcinoma of colon	ACSL4 AKR1B1 ANXA7 ARSA CD44 CEACAM5 CEACAM7 CYP1A1 CYP24A1 CYP3A4 DHRS11 DLD FUT10 FUT2 FUT3 FUT4 GALNT6 HSD17B7 LDHA LGALS3 LGALS4 MUTYH PGP PIK3CA PIK3CB PIK3CD PIK3CG PLA2G10 PLA2G2A PLAUR PLB1 PLCB1 PLD2 PTGS2 SDC2 SLC2A5 SLC5A1 SOAT1 ST6GAL1 SULT1E1 TM7SF2 UGT1A1	1048 1087 11226 151056 1543 1576 1591 1738 2182 231 23236 2524 2525 2526 283871 310 3939 3958 3960 410 4595 51478 5290 5291 5293 5294 5320 5329 5338 54658 5743 6383 6480 6518 6523 6646 6783 7108 79154 8399 84750 960	Homo sapiens (human)
DOID:5530	thymus squamous cell carcinoma Aliases: Epidermoid Thymic carcinoma	LY75	4065	Homo sapiens (human)
DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I Aliases: LGMD2I Limb-girdle muscular dystrophy due to FKRP deficiency MDDGC5 muscular dystrophy limb-girdle type 2I muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5 muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related	ACAN ACE ACHE AGK AGL ALDH7A1 ALOX12 ALPP APRT ATRNL1 B3GALNT2 B4GALNT2 B4GAT1 CD44 CHKA CHKB CRPPA CTNS DAG1 DCN DPEP1 DPM1 DPM2 DPM3 ENO1 FKRP FKTN GAA GK GLB1 GMPPB GNE HACD1 HPGDS HSPG2 IDH2 IMPA1 INPP5B INPP5K LARGE1 LARGE2 LGALS3 MBL2 MGAM PARP1 PIK3C2A PMM2 POGLUT1 POMGNT1 POMGNT2 POMK POMT1 POMT2 PRG2 PRKAA2 PYGM RGN RXYLT1 SDC2 SI SIRT2 SLC3A1 ST3GAL4 SYNJ1 SYNJ2	10020 10329 10585 11041 1119 1120 120071 124872 142 148789 1497 1605 1634 1636 176 178 1800 2023 2218 22933 239 250 2548 26033 2710 2720 27306 29925 29954 3339 3418 353 3612 3633 3958 4153 43 501 51763 5286 5373 54344 5553 55624 5563 55750 56983 5837 6383 6476 6484 6519 729920 79147 84197 84892 8813 8818 8867 8871 8972 9104 9200 9215 960	Homo sapiens (human)
DOID:11984	hypertrophic cardiomyopathy Aliases: hypertrophic obstructive cardiomyopathy	ABO ACACA ACADL ACADS ACADVL ACE ACSL1 ADPRH AGK AGL AGPAT2 ALDH2 ALG1 APRT ARSB ARSD ATP6V1A ATRN CALR3 CALR CAT CBR1 CBR3 CHST3 CNTN3 COG7 CPT1A CPT2 CS CYP11B2 CYP1A1 CYP1B1 CYP27B1 CYP2C19 CYP2C9 CYP2E1 DAG1 DCN DLD DPM3 ECHS1 EPHX2 FASN FIG4 FKRP FKTN FUT4 G6PD GAA GAPDH GBE1 GLA GLB1 GMPPB GNE GNPTAB GPC3 GPX3 GUSB GYG1 GYS1 HADH HADHA HADHB HAS3 HJV HPGDS HPSE ICAM1 IDH2 IDUA IGF2R IL1RL1 KL LDHA LGALS3 LPL MASP2 MBL2 MCAT MGAM MGAT1 MLYCD MMUT MTMR14 NAGA NAMPT NCAM1 NEU1 OLR1 PARP1 PCCA PCCB PDHA1 PGK1 PGM1 PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIKFYVE PKD1 PLA2G7 PMM2 PNPLA2 POMGNT1 POMK POMT1 PRKAA2 PTEN PTGS2 SCD5 SCD SDHA SDHB SDHD SGSH SI SIRT4 SLC2A10 SLC33A1 SLC5A1 SMUG1 SORD ST3GAL4 SUCLG1 SULT1E1 TPI1	10020 10135 10555 10585 10747 10855 125972 1374 1376 141 142 1431 148738 1543 1545 1557 1559 1571 1585 1594 1605 1634 1636 1738 178 1892 200576 2053 217 2180 2194 2218 23409 23417 23583 2526 2539 2548 2597 2632 2717 2719 2720 27306 27349 28 2878 2990 2992 29925 2997 3030 3032 3033 3038 31 33 3383 3418 3425 3482 35 353 37 3939 3958 4023 411 414 4153 4245 4594 4668 4684 4758 4973 5067 5095 5096 5160 523 5230 5236 5289 5290 5291 5293 5294 5310 5373 54344 55624 5563 55750 56052 57104 5728 5743 6319 6389 6390 6392 64419 6448 6476 6484 6523 6652 6783 7167 79147 79158 7941 79966 81031 811 84197 8455 847 873 874 8802 8972 9173 91949 9197 9365 9469 9896	Homo sapiens (human)
DOID:14175	von Hippel-Lindau disease Aliases: Hippel Lindau syndrome von Hippel-Lindau syndrome	ACHE APRT CHGA CYP19A1 CYP1B1 CYP2B6 IDH2 KLRD1 MUTYH PIK3CA PIK3CB PIK3CD PIK3CG PNPLA6 PRKAA2 PTEN PTGS2 PYGM SDHB SDHC SDHD SLC2A3 SMUG1 SORD TUSC3	10908 1113 1545 1555 1588 23583 3418 353 3824 43 4595 5290 5291 5293 5294 5563 5728 5743 5837 6390 6391 6392 6515 6652 7991	Homo sapiens (human)
DOID:0110123	Bardet-Biedl syndrome 1 Aliases: BBS1	INPP5E PIGX	54965 56623	Homo sapiens (human)
DOID:0080410	familial adenomatous polyposis 2 Aliases: MUTYH-associated polyposis MUTYH-related attenuated FAP MUTYH-related attenuated familial adenomatous polyposis MUTYH-related attenuated familial polyposis coli	CEACAM5 CEMIP MUTYH	1048 4595 57214	Homo sapiens (human)
DOID:13405	cardiac sarcoidosis	CALR SMUG1	23583 811	Homo sapiens (human)
DOID:1025	tuberculoid leprosy Aliases: Smooth leprosy type T leprosy	ICAM1 ICAM2 VCAM1	3383 3384 7412	Homo sapiens (human)
DOID:0060449	gelatinous drop-like corneal dystrophy Aliases: GDCD corneal amyloidosis primary familial amyloidosis of the cornea subepithelial amyloidosis of the cornea	GGT1	2678	Homo sapiens (human)
DOID:277	chorioangioma Aliases: Placental hemangioma	C1GALT1C1 CALR CD14 CTSA DPM1 GAS1 GPC6 HSD17B2 IDH1 IDH2 IGF2R IL18R1 LGALS9 MAG PIGF PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PNPLA2 PNPLA6 PTEN SDHD	10082 10908 2619 29071 3294 3417 3418 3482 3965 4099 5281 5290 5291 5293 5294 5310 5476 57104 5728 6392 811 8809 8813 929	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:5693	adult liposarcoma	CPM FASN GPNMB PIK3CA PIK3CB PIK3CD PIK3CG PNPLA2 PNPLA3 PTEN SDC1 SMUG1 STS	10457 1368 2194 23583 412 5290 5291 5293 5294 57104 5728 6382 80339	Homo sapiens (human)
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)
DOID:2321	obsolete dyspepsia	AGA CD14 CHGA COMT CYP2C19 GGT1 PTGDS PTGS1 PTGS2 UGT1A9	1113 1312 1557 175 2678 54600 5730 5742 5743 929	Homo sapiens (human)
DOID:4284	anal margin carcinoma Aliases: Perianal skin carcinoma	CEACAM5 CEACAM7 LIPA PIK3CA PIK3CB PIK3CD PIK3CG PTEN SMUG1	1048 1087 23583 3988 5290 5291 5293 5294 5728	Homo sapiens (human)
DOID:0070086	schizophrenia 10 Aliases: SCZD10	ALPL CERK	249 64781	Homo sapiens (human)
DOID:4012	papillary transitional carcinoma Aliases: Papillary transitional cell carcinoma	AKR1C3 PKM PTEN	5315 5728 8644	Homo sapiens (human)
DOID:1919	Lesch-Nyhan syndrome Aliases: Complete hypoxanthine-guanine phosphoribosyltransferase deficiency HG-PRT deficiency Hypoxanthine-guanine phosphoribosyltransferase deficiency Hypoxanthine-guanine-phosphoribosyltransferase deficiency Lesch - Nyhan syndrome X-linked hyperuricemia deficiency of IMP pyrophosphorylase hypoxanthine guanine phosphoribosyltransferase deficiency	APRT HPRT1 PNP	3251 353 4860	Homo sapiens (human)
DOID:28	endocrine system disease	B4GALT1 GAD1 PDIA3	2571 2683 2923	Homo sapiens (human)
DOID:0111375	fetal akinesia deformation sequence syndrome Aliases: FADS Pena-Shokeir syndrome type 1 arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome fetal akinesia sequence foetal akinesia deformation sequence syndrome foetal akinesia sequence	AGRN CNTN1 DPAGT1 GBA1 GBE1 PDHA1 PIGS	1272 1798 2629 2632 375790 5160 94005	Homo sapiens (human)
DOID:10457	Legionnaires' disease Aliases: Infection by Legionella pneumophilia Legionella Legionella pneumonia Legionnaire's disease	MBL2	4153	Homo sapiens (human)
DOID:3222	causalgia Aliases: Complex regional pain syndrome, type II	SMUG1	23583	Homo sapiens (human)
DOID:3127	proctitis	CALR CAT CEACAM5 CEACAM6 CEACAM7 COG6 GP2 LYZ MUTYH PARP1	1048 1087 142 2813 4069 4595 4680 57511 811 847	Homo sapiens (human)
DOID:4415	fibrous histiocytoma Aliases: Fibroxanthoma benign fibrous histiocytoma	SMUG1	23583	Homo sapiens (human)

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