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 **1101 - 1125** of **7942** in total

« First

‹ Prev

…

41

42

43

44

45

46

47

48

49

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲
DOID:2226	myeloproliferative neoplasm Aliases: CMPD CMPD, U chronic myeloproliferative disease	ACE ALOX12 ALOX5 CALR CAT CD177 CD33 CD44 CEL CHI3L1 CHIT1 CYP3A4 FUT1 FUT4 G6PC1 G6PD GPX1 GUSB HPRT1 HPSE IDH1 IDH2 IDS IL18R1 INPP5D LGALS1 LGALS3 MUTYH NAAA OGG1 PAFAH1B1 PARP1 PCYT1A PFKFB3 PIGA PIK3CA PIK3CB PIK3CD PIK3CG POFUT1 SIGLEC7 SOAT1	1056 10855 1116 1118 142 1576 1636 23509 239 240 2523 2526 2538 2539 27036 27163 2876 2990 3251 3417 3418 3423 3635 3956 3958 4595 4968 5048 5130 5209 5277 5290 5291 5293 5294 57126 6646 811 847 8809 945 960	Homo sapiens (human)
DOID:10175	optic papillitis Aliases: papillitis	CD38 ENO2 IDS SHMT1	2026 3423 6470 952	Homo sapiens (human)
DOID:0050156	idiopathic pulmonary fibrosis Aliases: FIBROCYSTIC PULMONARY DYSPLASIA IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL cryptogenic fibrosing alveolitis	ACE AKT1 ALOX5 ALPI ALPP ANXA5 ATP6AP2 B3GAT3 CD248 CD55 CEACAM5 CEACAM7 CEL CEMIP CHI3L1 CTSA CYP2C9 DCN ELOVL6 ENPP2 FCGR3B FOLR2 GGT1 GLB1 HK2 HS6ST1 HS6ST2 ICAM1 IL18R1 IL1RL1 KL KLRK1 L1CAM LCLAT1 LDHA LGALS1 LGALS3 LTA4H MICA MPG MRC1 NEU1 NT5E PARP1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKD2 PRKAA2 PTEN PTGS1 PTGS2 SDC1 SDC2 SDC4 SEMA7A SFTPA1 SFTPA2 SFTPC SFTPD SHMT2 SIRT6 SLC27A5 SLC2A10 SLC2A5 SMUG1 SOAT1 SPHK1 SULF2 TM7SF2 VCAM1 VCAN	100507436 10159 1048 1056 1087 10998 1116 142 1462 1559 1604 1634 1636 207 2215 22914 2350 23583 240 248 250 253558 26229 2678 2720 308 3099 3383 3897 3939 3956 3958 4048 4350 4360 4758 4907 51548 5168 5290 5291 5293 5294 5310 5311 5476 5563 55959 57124 57214 5728 5742 5743 6382 6383 6385 6440 6441 6472 6518 653509 6646 7108 729238 7412 79071 81031 83666 8482 8809 8877 90161 9173 9365 9394	Homo sapiens (human)
DOID:4072	duodenum disease Aliases: duodenal disease duodenum disorder	CAT CEACAM5 CEACAM7 CYP2C9 DHRS11 HSD17B7 OGG1 PTEN PTGS2	1048 1087 1559 4968 51478 5728 5743 79154 847	Homo sapiens (human)
DOID:11725	Cornelia de Lange syndrome Aliases: Brachmann de Lange syndrome De Lange syndrome	ACADS AMT ARSA ARSD B4GALT7 BAAT CAT CHPT1 CYP11A1 DAG1 DCN DHDDS EXT1 FOLR1 GALNT14 GAPDH GCSH GLB1 GLDC GPI HSPG2 KL OGG1 PARP1 PGAM2 PIK3CA PIK3CB PIK3CD PIK3CG PRNP PTEN SGPL1 SMC3 STS TNKS XYLT2	11285 142 1583 1605 1634 2131 2348 2597 2653 2720 2731 275 2821 3339 35 410 412 414 4968 5224 5290 5291 5293 5294 5621 56994 570 5728 64132 79623 79947 847 8658 8879 9126 9365	Homo sapiens (human)
DOID:3953	adrenal gland cancer Aliases: adrenal cancer adrenal neoplasm malignant Adrenal tumor malignant neoplasm of adrenal gland neoplasm of adrenal gland tumor of the Adrenal gland	ACACA ACE ACO1 APRT CAT CD44 CHGA CHST3 CNTN4 COMT CS CYP11B1 CYP11B2 CYP17A1 CYP19A1 CYP21A2 CYP4F3 DGCR2 DHCR24 DHRS11 DLST FH G6PD GUSB HPSE HSD11B1 HSD17B7 IDH1 IDH2 L1CAM LGALS3 MDH2 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PKD2 PTEN PTGS2 SDHA SDHB SDHC SDHD SLC33A1 SMPD1 SMUG1 SORD	10855 1113 1312 142 1431 152330 1584 1585 1586 1588 1589 1636 1718 1743 2271 23583 2539 2990 31 3290 3417 3418 353 3897 3958 4051 4191 48 51478 5290 5291 5293 5294 5311 5728 5743 6389 6390 6391 6392 6609 6652 79154 847 9197 9469 960 9993	Homo sapiens (human)
DOID:0111630	familial erythrocytosis 8 Aliases: BPGM deficiency DPGM deficiency ECYT8 bisphosphoglycerate mutase deficiency bisphosphoglyceromutase deficiency diphosphoglycerate mutase deficiency of erythrocyte hemolytic anemia due to diphosphoglycerate mutase deficiency	BPGM	669	Homo sapiens (human)
DOID:0070263	congenital disorder of glycosylation type IIk Aliases: CDG IIk CDG syndrome type IIk CDG2K CDGIIdk Carbohydrate deficient glycoprotein syndrome type IIk Congenital disorder of glycosylation type 2k TMEM165-CDG	TMEM165	55858	Homo sapiens (human)
DOID:848	arthritis Aliases: Inflammatory disorder of joint	ABAT ABO ACAA2 ACACA ACAN ACE ACLY ACO1 ACSL4 ACSL6 AGA AKR1C1 AKR1C2 ALDOA ALOX15 ALOX5 ALPL ANXA5 APRT ARSA ART1 ASAH1 B3GAT1 B4GALNT3 B4GALT7 BCKDHA BST2 CALR CAT CD14 CD209 CD22 CD248 CD38 CD44 CD55 CD74 CEMIP CH25H CHAT CHGA CHI3L1 CHI3L2 CHST11 CHST13 CHST3 CHST4 CLC CLEC12A CLEC3A CLEC4E CLEC5A CLEC7A CNTN1 CNTN2 COG5 COL9A2 COMT CPT2 CSPG4 CYP19A1 CYP1B1 CYP2B6 CYP7B1 DCN DCXR DPEP1 ENO1 ENPP1 ENPP2 EXT1 EXT2 FASN FCGR3B FCN1 FH FMOD FUT1 FUT2 GAL3ST1 GANAB GAPDH GBA1 GCK GGT1 GLA GLB1 GLO1 GLT8D1 GMDS GPC3 GPD1L GPI GPNMB GPX1 GUSB GYS1 HADHA HAS1 HIBCH HJV HK1 HK2 HMMR HPGDS HPRT1 HPSE HS6ST2 HSD11B1 HSD11B2 HYAL1 HYAL2 ICAM1 IDH2 IDH3A IL18R1 IL1R1 IL1RL2 INPP5D ISYNA1 KL KLRB1 LACC1 LAYN LCTL LGALS1 LGALS3 LGALS8 LGALS9 LYZ MASP1 MBL2 MMP17 MMP25 MRC1 MUTYH NAAA NAMPT NCAM1 NT5E OCRL OLR1 OPCML PAPSS2 PARP1 PDHA1 PDIA3 PFKFB3 PGAM1 PIGQ PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G10 PLA2G1B PLA2G2A PLA2G4A PLA2G4F PLA2G6 PLAUR PLB1 PLCD1 PLCG1 PLD1 PNPLA3 PRKAA2 PRNP PTEN PTGDS PTGES PTGS1 PTGS2 RECK RENBP SCD5 SDC1 SDC4 SDHA SELE SELL SFTPD SGSH SHMT2 SIGLEC7 SIGLEC9 SIRT2 SIRT6 SLC17A5 SLC26A2 SLC35A1 SLC39A8 SMUG1 SOAT1 SPHK1 SPHK2 SRGN ST3GAL5 STS SULF1 SULF2 TKTL1 TLR4 TM7SF2 TNKS TPI1 UST VCAM1 VCAN VTCN1 XYLT1	10090 10135 10143 10164 10449 10457 10466 10559 10855 1103 1113 1116 1117 11285 1178 1272 1298 1312 1376 142 143903 144811 1462 1464 148738 151056 1545 1555 1588 160364 1604 1634 1636 1645 1646 166012 175 176 18 1800 1836 197021 2023 2131 2132 2182 2194 2215 2219 226 2271 22933 23171 23193 23213 23305 2331 23583 23601 240 246 249 2523 2524 255189 2597 26253 26275 2629 2645 26503 2678 27036 27087 27163 2717 27180 2719 2720 27306 2739 2762 28 2821 283358 2876 2923 2990 2997 3030 3036 308 30835 3098 3099 31 3161 3251 3290 3291 3373 3383 3418 3419 353 3554 3635 3820 3956 3958 3964 3965 4069 410 412 4153 417 427 4326 4360 4595 4684 47 48 4907 4952 4973 4978 50515 51181 51477 51548 5160 5167 5168 5209 5223 5290 5291 5293 5294 5315 5319 5320 5321 5329 5333 5335 5337 5552 5563 55830 55959 5621 5648 56848 57124 57214 5728 5730 5742 5743 593 5973 6382 6385 6389 6401 6402 64116 64131 64386 6441 6448 64581 6472 6646 684 6900 7099 7108 7167 7412 79679 79966 80339 811 8277 8398 8399 8434 847 8658 8692 8808 8809 8869 8877 90161 9023 9060 9091 929 933 9365 9420 9469 9514 952 9536 960 972	Homo sapiens (human)
DOID:0110848	xeroderma pigmentosum group F Aliases: XP group F XP6 XPF xeroderma pigmentosum VI	CAT COMT CYP1B1 HPGDS HPRT1 OGG1 PTEN SMUG1 TALDO1 XYLT2	1312 1545 23583 27306 3251 4968 5728 64132 6888 847	Homo sapiens (human)
DOID:10376	amblyopia Aliases: lazy eye	B3GAT3 CHST3 COL9A2 GALC GMPPB OCRL OGT PIGN PPARGC1A XYLT2	10891 1298 23556 2581 26229 29925 4952 64132 8473 9469	Homo sapiens (human)
DOID:474	histiocytoid hemangioma Aliases: Angiolymphoid hyperplasia with eosinophilia epithelioid haemangioma epithelioid 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:0080443	developmental and epileptic encephalopathy 21 Aliases: DEE21 early infantile epileptic encephalopathy 21	CACNA2D2	9254	Homo sapiens (human)
DOID:0070117	Meckel syndrome 3 Aliases: MKS3 Meckel-Gruber syndrome, type 3	ALG8 ALG9 ARF4 PGD PKD1 PKD2 UMOD	378 5226 5310 5311 7369 79053 79796	Homo sapiens (human)
DOID:0110202	Charcot-Marie-Tooth disease dominant intermediate A Aliases: CMTDIA Charcot-Marie-Tooth neuropathy dominant intermediate A DI-CMTA autosomal dominant intermediate Charcot-Marie-Tooth disease type A	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)
DOID:0110822	hereditary spastic paraplegia 77 Aliases: SPG77 autosomal recessive spastic paraplegia 77	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:0111672	primary hyperoxaluria type 3 Aliases: HP3 PH III primary hyperoxaluria type III	HOGA1	112817	Homo sapiens (human)
DOID:4479	pseudohypoaldosteronism	MRC1	4360	Homo sapiens (human)
DOID:8446	intussusception Aliases: Intussusception of intestine Invagination of intestine or colon	PCYT1A PTEN SLC35G1	159371 5130 5728	Homo sapiens (human)
DOID:13206	nodular prostate	ACE ACSS2 AKR1B10 ALDH7A1 ALOX12 ALOX15 ALOX15B ALOX5 AMACR ANXA7 CANX CAT CD177 CD44 COMT CYP11A1 CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP2B6 CYP3A4 CYP3A5 EFNA2 ELOVL6 ENO2 ENPP1 ENPP2 GALNT3 GGT1 GLCE GOLPH3 GPC1 HMMR HPGDS HPSE HSD17B1 HSD17B2 HSD17B3 HSD17B7 ISYNA1 KLB LDHA LGALS8 LPL LYZ MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PLD1 PRG2 PTEN PTGS2 RECK RENBP SLC33A1 SRD5A1 SRD5A2 STS SULF1 SULT1E1 UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT2B15 UGT2B17 VCAN	10855 1312 1462 152831 1543 1545 1555 1576 1577 1583 1586 1588 1636 1943 2026 23213 23600 23659 239 240 246 247 2591 26035 2678 27306 2817 310 3161 3292 3293 3294 3939 3964 4023 4069 412 4360 501 51477 51478 5167 5168 5290 5291 5293 5294 5337 54575 54576 54577 54578 54657 54658 5553 55902 57016 57126 5728 5743 5973 64083 6715 6716 6783 7366 7367 79071 821 8434 847 9197 960	Homo sapiens (human)
DOID:90	degenerative disc disease Aliases: cervical disc degenerative disease intervertebral disc degeneration lumbar disc degeneration vertebral disc disease	ACAN ADH1B CD74 COL9A2 COMT DGCR2 GAS1 GPC6 GSK3B ICAM1 IDH1 IDH2 IL18RAP LDHA LGALS3 PGP PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGS2 SIRT2 SIRT6 SRGN SULF1 TIGAR XYLT1	10082 125 1298 1312 176 22933 23213 2619 283871 2932 3383 3417 3418 3939 3958 51548 5290 5291 5293 5294 5552 57103 5728 5743 64131 8807 972 9993	Homo sapiens (human)
DOID:8353	epithelioid malignant peripheral nerve sheath tumor Aliases: epithelioid MPNST malignant epithelioid neoplasm of the peripheral nerve Sheath	CD38 CD44 CEACAM5 CHSY1 DCN G6PD HMMR IL1R1 LGALS1 NCAM1 PARP1 PARP2 PIK3CA PIK3CB PIK3CD PIK3CG PTEN RECK SMUG1 SOAT1	10038 1048 142 1634 22856 23583 2539 3161 3554 3956 4684 5290 5291 5293 5294 5728 6646 8434 952 960	Homo sapiens (human)
DOID:0081001	Cowden syndrome 5	PIK3CA	5290	Homo sapiens (human)
DOID:936	brain disease Aliases: encephalopathy	ACE ACHE ACSF3 AMACR AMT APRT ARSA ATP6V1A CAT CEL CLN5 COG8 CPT2 CYB5R3 CYP2B6 CYP2R1 CYP46A1 DLD ENO2 FCN2 FDPS FH FUT8 GBA1 GCDH GCSH GLDC GLUL GLYCTK HIBCH HMGCL HPGDS IDH3A IDS LGALS3 MCAT NCAN NTNG1 OGG1 PARP9 PDHX PGAP1 PIGA PIGT PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G6 PLCB1 POMT1 PPT1 PRNP PTEN PTGES PTGS2 RTN4R SDC2 SDHA SLC27A5 SLC2A3 SLC33A1 SLC35A1 SLC35A2 SMUG1 SUCLG1 SYNJ1 TM7SF2 UGT1A1 VCAN	10559 1056 10585 10858 10998 120227 1203 132158 1376 1462 1463 1555 1636 1727 1738 197322 2026 2220 2224 2271 22854 23236 23583 23600 2530 26275 2629 2639 2653 27306 2731 27349 275 2752 3155 3419 3423 353 3958 410 43 4968 51604 523 5277 5290 5291 5293 5294 5315 54658 5538 5621 5728 5743 6383 6389 65078 6515 7108 7355 80055 8050 83666 8398 84342 847 8802 8867 9197 9536	Homo sapiens (human)
DOID:0110484	autosomal recessive nonsyndromic deafness 26 Aliases: DFNB26 autosomal recessive deafness 26	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)

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