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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 **3301 - 3325** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:13620	patent foramen ovale Aliases: Atrial septal defect within oval fossa Defect, Patent or persistent, ostium secundum Ostium secundum type atrial septal defect Persistent ostium secundum foramen ovale patent	ACADVL ALG12 ARSA ARSD ATP6V1A B3GALT6 B3GAT3 B3GLCT CAT CFC1 CHST14 CHST3 COMT CYP11A1 CYP11B2 CYP1B1 CYP2E1 DSE FIG4 FKTN G6PC3 GAA GPC3 GPC6 MASP1 MMUT PCYT1A PIGA PIGN PIGQ PLD1 PTEN RENBP SMC3 TALDO1 TGDS TKT XYLT2	10082 113189 126792 1312 145173 1545 1571 1583 1585 2218 23483 23556 2548 26229 2719 29940 37 410 414 4594 5130 523 5277 5337 55997 5648 5728 5973 64132 6888 7086 79087 847 9091 9126 92579 9469 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:3044	food allergy Aliases: food hypersensitivity	CD14 FCER2	2208 929	Homo sapiens (human)	DisGeNET
DOID:1080	filariasis Aliases: disease due to superfamily Filarioidea	ABO CHIT1 GLB1 LGALS2 MBL2	1118 2720 28 3957 4153	Homo sapiens (human)	DisGeNET
DOID:1858	McCune Albright syndrome Aliases: fibrous dysplasia of bone osteitis fibrosa disseminata polyostotic fibrous dysplasia	ACSS2 AMY1A AMY1B AMY1C APRT ENPP1 PLA2G15 SUCLG1	23659 276 277 278 353 5167 55902 8802	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:3355	fibrosarcoma Aliases: Fibrocytic tumor fibrosarcoma of soft tissue fibrous tissue neoplasm	ACE AKR1A1 AKR1B1 ANXA5 APRT CD44 CHST3 DLD EBP GLB1 GLO1 GPI HK1 HPRT1 HSPG2 ICAM1 IDH1 KLRK1 MMP25 MTAP NAMPT PARP1 PC PIK3CA PIK3CB PIK3CD PIK3CG PSAP PTEN PTGES3 PTGS2 RECK SDC1 SDC2 SIGLEC7 SLC26A2 SMPD1 STS	10135 10327 10682 10728 142 1636 1738 1836 22914 231 27036 2720 2739 2821 308 3098 3251 3339 3383 3417 353 412 4507 5091 5290 5291 5293 5294 5660 5728 5743 6382 6383 64386 6609 8434 9469 960	Homo sapiens (human)	DisGeNET
DOID:631	fibromyalgia	ACADL ACE ACHE APRT CALR CAT CD22 CNTN3 COMT CPT2 CRPPA DSE ENO1 ENO3 ENPP2 EXT1 FKRP FKTN FMOD FOLR2 GLA GOLPH3 GPX1 HADHA HADHB HPGDS HSD11B1 HSPG2 KLRC1 KLRD1 L1CAM LALBA LDHA LGALS8 LPIN1 LPIN2 NT5E PCYT1A PIGT PIK3C2A PNPLA2 POMT1 PRKAA2 PTGS2 SELL SLC17A5 VCAM1	10585 1312 1376 1636 2023 2027 2131 2218 23175 2331 2350 26503 2717 27306 2876 29940 3030 3032 3290 33 3339 353 3821 3824 3897 3906 3939 3964 43 4907 5067 5130 51604 5168 5286 5563 57104 5743 6402 64083 729920 7412 79147 811 847 933 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:3086	gingival overgrowth Aliases: Gingival enlargement	AGA CYP2C9 DHCR24 GLB1 GUSB IDUA MAN2B1 MGAT2 PIGA PIGN PIGS SC5D SLC17A5	1559 1718 175 23556 26503 2720 2990 3425 4125 4247 5277 6309 94005	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:9598	fasciitis	GAPDH PTGS2	2597 5743	Homo sapiens (human)	DisGeNET
DOID:668	myositis ossificans Aliases: Myisitis ossificans Ossification - muscle	APRT CD14 COMT DPEP1 ENPP2 GPC1 SDC2 SDC4	1312 1800 2817 353 5168 6383 6385 929	Homo sapiens (human)	DisGeNET DisGeNET
DOID:13374	fibrodysplasia ossificans progressiva Aliases: Stone Man Syndrome myositis ossificans progressiva progressive myositis ossificans progressive ossifying myositis	APRT CD14 COMT DPEP1 ENPP2 GPC1 SDC2 SDC4	1312 1800 2817 353 5168 6383 6385 929	Homo sapiens (human)	DisGeNET DisGeNET
DOID:5998	microglandular adenosis Aliases: Adenosis - breast Adenosis of the breast	ACE CEACAM5 CEACAM7 COMT CRLS1 CYP11A1 CYP17A1 CYP19A1 CYP1A1 CYP1B1 DCN GFRA1 GLA HSD17B1 INPP4B LPCAT1 MICA NCAM1 PTEN PTGS2 SDC3	100507436 1048 1087 1312 1543 1545 1583 1586 1588 1634 1636 2674 2717 3292 4684 54675 5728 5743 79888 8821 9672	Homo sapiens (human)	DisGeNET DisGeNET
DOID:10354	breast fibrocystic disease Aliases: Diffuse cystic mastopathy Fibrocystic disease of breast breast Fibrocystic Change	ACE CEACAM5 CEACAM7 COMT CRLS1 CYP11A1 CYP17A1 CYP19A1 CYP1A1 CYP1B1 DCN GFRA1 GLA HSD17B1 INPP4B LPCAT1 MICA NCAM1 PTEN PTGS2 SDC3	100507436 1048 1087 1312 1543 1545 1583 1586 1588 1634 1636 2674 2717 3292 4684 54675 5728 5743 79888 8821 9672	Homo sapiens (human)	DisGeNET DisGeNET
DOID:3891	placental insufficiency	ABO ACACA ACADVL ACE ACSL4 ADH1B AGA AKR1A1 AKR1B1 ALDH2 ALDH3A1 ALG12 ALG13 ALG1 ALG8 ANXA5 ATP6V0A2 ATP6V1A B3GLCT BCKDHA CALR CAT CD74 CEL CHPT1 CNTN1 COG1 COG4 COG5 COG6 COG7 COMT CPT1A CPT2 CRYL1 CYB5R3 CYP11A1 CYP11B1 CYP17A1 CYP19A1 CYP1A1 CYP2E1 CYP7A1 DCN DHCR24 DHCR7 DLAT FCN2 FCN3 FIG4 FKTN FUT8 G6PC1 GALC GALK1 GAPDH GAS1 GBA1 GCK GK GLUL GPC1 GPC3 GPI GPX1 H6PD HADH HADHA HADHB HAS2 HK1 HSD11B2 HSD17B1 IGF2R IL1RAPL1 KL KLRB1 LDHC LFNG LGALS2 LGALS3 LIPG LPL MAG MASP1 MBL2 MPI MTM1 MYORG NGLY1 OGDH PCK1 PDHA1 PDHX PDX1 PFKFB2 PIGF PIGG PIK3C2A PIK3CA PIK3CB PIK3CD PIK3CG PKD2 PLCG1 PLOD3 PNPLA6 POMT1 PPARGC1A PRKAA2 PRNP PRPS1 PTDSS1 PTEN PTGS2 SC5D SDC1 SDHA SDHB SDHD SIRT2 SLC26A2 SLC2A2 SLC2A3 SLC2A4 SLC33A1 SLC35A1 SLC35A2 SMC3 STT3B TALDO1 TGDS UGDH UPP1 VCAM1 VTCN1 XYLT1	10327 10466 10559 1056 10585 10891 10908 11141 125 1272 1312 1374 1376 145173 1543 1571 1581 1583 1584 1586 1588 1634 1636 1717 1718 1727 1737 175 1836 201595 217 218 2182 2218 2220 22933 231 23483 23545 2530 2538 2581 25839 2584 2597 2619 2629 2645 2710 2719 2752 28 2817 2821 2876 3030 3032 3033 3037 308 3098 31 3291 3292 3482 3651 37 3820 3948 3955 3957 3958 4023 4099 4153 4351 4534 4967 5105 51084 5160 5208 523 5281 5286 5290 5291 5293 5294 5311 5335 54872 5563 55768 56052 5621 5631 5648 56994 5728 5743 57462 57511 593 6309 6382 6389 6390 6392 64131 6514 6515 6517 6888 7355 7358 7378 7412 79053 79087 79679 79868 8050 811 847 8547 8985 9126 91949 9197 9365 9382 9388 9563 972 9791 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:11042	Felty's syndrome Aliases: Felty syndrome Rheumatoid arthritis with splenoadenomegaly and leukopenia	B3GAT1	27087	Homo sapiens (human)	DisGeNET
DOID:9452	steatotic liver disease Aliases: Fatty change of liver SLD Steatosis of liver alcoholic fatty liver fatty liver disease hepatic lipidosis hepatic steatosis	AACS ABO ACACA ACACB ACADL ACADM ACADVL ACAT1 ACE ACLY ACOX1 ACSL1 ACSL4 ACSL5 ACSS2 ADH1A ADH1B ADH4 ADIPOQ AGPAT1 AGPAT2 AKR1A1 AKR1B10 AKR1B1 AKR1D1 ALDH1A3 ALDH1B1 ALDH2 ALDOB ALOX12 ALOX5 ALPL ALPP APRT ART3 ATP6AP1 ATRNL1 B3GAT1 BAAT CAT CBR1 CD14 CD1D CD44 CDIPT CEL CERS1 CERS2 CERS6 CHIT1 CHKA CHPT1 CMAS CPT1A CPT1B CPT1C CPT2 CS CTSA CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP27B1 CYP2B6 CYP2E1 CYP2J2 CYP2R1 CYP3A4 CYP4A11 CYP4F2 CYP4F3 CYP7A1 CYP7B1 CYP8B1 DCN DDOST DGAT1 DGAT2 DHDDS DHRS11 DLAT EBP ELOVL2 ELOVL5 ELOVL6 ENO2 ENO3 ENPP1 ETNPPL FADS1 FADS2 FASN FBP1 FCGR3B FDFT1 FOLR2 FUT4 G6PC1 G6PD GCK GGT1 GLB1 GLUL GPAM GPC3 GPD1 GPD1L GPI GPX1 H6PD HACD1 HADH HADHA HADHB HAS3 HJV HKDC1 HPGDS HPSE HSD11B1 HSD17B4 HSD17B7 HSPG2 HTR2A ICAM1 IDH2 INPP5D INS ISYNA1 KDSR KHK KLB LALBA LCAT LEP LGALS3 LIPA LPIN1 LPL MBOAT7 MCAT MGLL MIOX MLYCD MOGAT1 MOGAT3 MPI MRC1 NAAA NAMPT NCAN NEIL1 NEU1 OGT OPCML PARP1 PARP2 PC PCK1 PCK2 PDIA3 PEMT PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G6 PLA2G7 PLCG1 PMM2 PNPLA2 PNPLA3 PNPLA6 PPARA PPARGC1A PPP1R3B PPP1R3C PPP1R3G PRKAA2 PSMD10 PTEN PTGS1 PTGS2 REG3G RENBP SARM1 SCD SCP2 SELE SELL SGMS2 SIGLEC1 SIGLEC7 SIRT2 SIRT4 SIRT6 SLC17A5 SLC27A5 SLC2A12 SLC2A2 SLC2A4 SLC2A8 SLC35A2 SMPD1 SMUG1 SOAT2 SORD SPHK2 SQLE ST3GAL4 ST6GAL1 ST8SIA4 STS SULF1 SULT1E1 THEM5 TM7SF2 TMEM199 TREH UCP2 UGCG UGT1A10 UGT1A4 UGT1A6 UGT1A7 UGT1A8 UGT2B4 VCAM1 VNN1 XYLT2	10038 10135 10327 10400 10423 10554 10555 1056 10682 10715 10855 10891 10908 10998 1118 11181 1119 11343 116255 120227 124 125 126129 127 130120 1374 1375 1376 142 1431 1463 147007 148738 152831 154091 1543 1544 1545 1555 1571 1573 1576 1579 1581 1582 1586 1588 1594 1634 1636 1650 166929 1737 2026 2027 217 2180 2182 219 2194 220 2203 2215 2222 229 22933 23098 231 23171 23175 23213 23409 23417 2350 23583 239 240 249 250 2526 2531 253782 2538 2539 26033 2645 26503 2678 27036 27087 27163 2719 2720 27306 27349 2752 28 2819 2821 284486 2876 2923 29956 29988 3030 3032 3033 3038 31 32 3290 3295 33 3339 3356 3383 34 3418 346606 353 3630 3635 37 3795 38 3906 3931 3952 3958 3988 3992 4023 4051 412 419 4351 4360 47 4758 4978 5091 51 5105 5106 51477 51478 51548 5167 51703 5236 5290 5291 5293 5294 5315 5335 537 5373 54575 54576 54577 54578 5465 54657 5476 54898 5507 55586 5563 55902 55907 56848 56994 570 57016 57104 5716 5728 5742 5743 57678 5973 60481 6319 6342 6401 6402 64132 6480 6484 64850 648791 6514 6517 65985 6609 6614 6652 6713 6718 6783 7108 7351 7355 7357 7363 7412 7903 79071 79143 79154 7941 79660 79661 79947 80201 80339 8398 8435 84649 847 8473 8529 8694 873 8876 912 9200 929 9370 9415 9420 9563 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:885	fascioliasis Aliases: Fasciola hepatica infection Infection by Fasciola Liver flukes Sheep liver fluke infection	HPGDS PSAP SLC17A5	26503 27306 5660	Homo sapiens (human)	DisGeNET
DOID:13636	Fanconi anemia Aliases: Fanconi anaemia Fanconi pancytopenia Fanconi panmyelopathy Fanconi's anaemia Fanconi's anemia	ADH5 ALDH2 ANXA7 CAT CD33 CD38 CD44 CD48 CTNS CYP11A1 CYP2B6 ELOVL6 ENO1 FUT1 GCK HPGDS HPRT1 ICAM1 LPL ME1 MRC1 NCAM1 NEIL1 NEIL3 NTHL1 OCRL PARP1 PFKFB3 PRKAA2 PTEN SOAT1 TIGAR TNF VCAM1	128 142 1497 1555 1583 2023 217 2523 2645 27306 310 3251 3383 4023 4199 4360 4684 4913 4952 5209 55247 5563 57103 5728 6646 7124 7412 79071 79661 847 945 952 960 962	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:5684	spondyloepimetaphyseal dysplasia, Sponastrime type Aliases: Spondylar and nasal Alterations-Striated Metaphyses syndrome sponastrime dysplasia	CTNS CYP51A1 EHHADH GPX3 IGF2R NAGLU OCRL SLC2A2 VNN1 VNN2	1497 1595 1962 2878 3482 4669 4952 6514 8875 8876	Homo sapiens (human)	DisGeNET DisGeNET
DOID:1062	Fanconi syndrome Aliases: Congenital Fanconi syndrome De Toni-Fanconi syndrome Fanconi-de Toni syndrome Fanconi-de-Toni syndrome Infantile nephropathic cystinosis Lignac-Fanconi syndrome adult Fanconi Anemia adult Fanconi syndrome deToni Fanconi syndrome	AGPAT2 CTNS CYP51A1 EHHADH GPX3 IGF2R NAGLU OCRL SLC2A2 SLC5A1 VNN1 VNN2	10555 1497 1595 1962 2878 3482 4669 4952 6514 6523 8875 8876	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:2231	factor XII deficiency Aliases: Factor XII deficiency disease Hageman Factor deficiency deficiency, Hageman	MGAT2 PGAP1	4247 80055	Homo sapiens (human)	DisGeNET
DOID:1756	facial nerve disease	ACADS ACSL4 AGRN ALG13 ALG14 ALG2 ASAH1 CHKB DPAGT1 FKRP GFPT1 GMPPB GNE HPGDS IL1RAPL1 LARGE1 MTM1 MTMR14 MTMR2 POMT1 POMT2 PTDSS1 SMUG1	10020 10585 11141 1120 1798 199857 2182 23583 2673 27306 29925 29954 35 375790 427 4534 64419 79147 79868 85365 8898 9215 9791	Homo sapiens (human)	DisGeNET
DOID:12506	Bell's palsy Aliases: Bell palsy Bell's (facial) palsy	ACADS ACSL4 AGRN ALG13 ALG14 ALG2 ASAH1 CHKB DPAGT1 FKRP GFPT1 GMPPB GNE HPGDS IL1RAPL1 LARGE1 MTM1 MTMR14 MTMR2 POMT1 POMT2 PTDSS1 SMUG1	10020 10585 11141 1120 1798 199857 2182 23583 2673 27306 29925 29954 35 375790 427 4534 64419 79147 79868 85365 8898 9215 9791	Homo sapiens (human)	DisGeNET DisGeNET
DOID:13934	facial paralysis Aliases: Facial Palsy	ACADS ACSL4 AGRN ALG13 ALG14 ALG2 ASAH1 CHKB DPAGT1 FKRP GFPT1 GMPPB GNE HPGDS IL1RAPL1 LARGE1 MTM1 MTMR14 MTMR2 POMT1 POMT2 PTDSS1 SMUG1	10020 10585 11141 1120 1798 199857 2182 23583 2673 27306 29925 29954 35 375790 427 4534 64419 79147 79868 85365 8898 9215 9791	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:1757	facial hemiatrophy Aliases: PARRY-ROMBERG SYNDROME	CD38	952	Homo sapiens (human)	DisGeNET
DOID:2174	ocular cancer Aliases: Ocular tumor eye neoplasm malignant eye neoplasm neoplasm of eye neoplasm of eye proper	FASN LIPG	2194 9388	Homo sapiens (human)	DisGeNET DisGeNET

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