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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 **3801 - 3825** of **7942** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism
DOID:11476	osteoporosis	Igf2 Lep Lepr Myc Pcna	24483 24536 24577 25608 25737	Rattus norvegicus (Norway rat)
DOID:11476	osteoporosis	ABO ACE ACHE AGPAT2 AKR1A1 AKR1B1 AKR1C4 AKR1D1 ALDH2 ALDH7A1 ALOX12 ALOX15 ALPL ALPP ARSA ASAH1 ATRNL1 B3GALT6 B3GAT3 CAT CD14 CD38 CD44 CHST3 CLC COMT CPT1A CYP11A1 CYP11B1 CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP3A4 DDOST DGCR2 DPEP1 ENO1 ENPP1 EXT1 FASN FDPS G6PC1 GALNS GALNT3 GALT GAPDH GK GLB1 GLO1 GPAA1 GPC6 GPD2 GPLD1 GPNMB GPX1 HJV HPGDS HPRT1 HPSE HS6ST1 HSD11B1 HSD11B2 HSD17B1 HSD17B2 HSD17B4 HSD3B2 HSD3B7 HSPG2 ICAM1 IDH2 IDUA IGF2 INPP4B IRS2 ITLN1 KL LCT LEP LEPR LGALS8 LRP5 MAPK14 MBL2 MGLL MMP17 NAMPT NDUFAB1 NGLY1 OXCT1 PCCA PCCB PCNA PGLS PIGT PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1B PKM PLCG2 PMM2 PNP PRKAA2 PTEN SGMS2 SIGLEC15 SIRT2 SIRT6 SLC26A2 SLC37A4 SMPD1 SMUG1 SOAT1 ST3GAL4 TM7SF2 TMEM165 TPI1 UGT2B17 UMOD VCAM1 XXYLT1 XYLT2	10082 10135 10327 10457 10555 10855 1109 11343 1178 126792 1312 1374 1432 148738 152002 1543 1545 1555 1576 1583 1584 1586 1588 1591 1593 1594 1636 1650 166929 1800 1836 2023 2131 217 2194 2224 22933 231 23583 239 246 249 250 2538 2542 25796 2588 2591 2592 2597 26033 26229 2710 2720 27306 2739 28 2820 2822 284266 2876 3251 3284 3290 3291 3292 3294 3295 3339 3383 3418 3425 3481 3938 3952 3953 3964 4041 410 4153 427 43 4326 4706 4860 501 5019 5095 5096 5111 51548 51604 5167 5290 5291 5293 5294 5315 5336 5373 55600 5563 55768 55858 5728 64132 6484 6609 6646 6718 7108 7167 7367 7369 7412 80270 8395 847 8660 8733 8821 929 9365 9394 9469 952 960 9993	Homo sapiens (human)
DOID:11476	osteoporosis	Igf2 Lep Lepr Lrp5 Mapk14 Myc Pcna	16002 16846 16847 16973 17869 18538 26416	Mus musculus (house mouse)
DOID:1148	polydactyly Aliases: postaxial polydactyly	ACHE DHCR7 EBP GPC3 HADHB INPP5E PIGX PIK3CA PNPLA6 PTEN SC5D UMOD	10682 10908 1717 2719 3032 43 5290 54965 56623 5728 6309 7369	Homo sapiens (human)
DOID:11481	constrictive pericarditis	SMUG1	23583	Homo sapiens (human)
DOID:11482	hemopericardium Aliases: Haemopericardium	ACADVL ACE ALG9 CAT GBA1 PMM2 PTGS2 SMUG1	1636 23583 2629 37 5373 5743 79796 847	Homo sapiens (human)
DOID:11486	Horner's syndrome Aliases: Bernard Horner syndrome Horner syndrome cervical sympathetic paralysis	ACE ACHE ATP6AP2 COMT GLA PIK3CA PIK3CB PIK3CD PIK3CG PRNP SPTLC1 TM7SF2	10159 10558 1312 1636 2717 43 5290 5291 5293 5294 5621 7108	Homo sapiens (human)
DOID:115	cardiac tamponade Aliases: Rose's tamponade pericardial tamponade	PCYT1A SMUG1 SOAT1	23583 5130 6646	Homo sapiens (human)
DOID:11502	mitral valve insufficiency Aliases: Congenital insufficiency of mitral valve Mitral valve incompetence congenital mitral insufficiency congenital mitral regurgitation mitral regurgitation	ABO ACE AGA B3GALT6 B3GAT3 CHST3 DSE ENPP1 G6PC3 GLA HADHA HADHB IDUA PLD1 PRKAA2 SCD XYLT1 XYLT2	126792 1636 175 26229 2717 28 29940 3030 3032 3425 5167 5337 5563 6319 64131 64132 92579 9469	Homo sapiens (human)
DOID:11503	diabetic autonomic neuropathy	ACE ACSL1 AKR1B1 CAT ENO2 GLO1 GPX1 PARP1 PMM2 PNPLA6 PTEN PTGS2 RENBP SMPD1 ST3GAL4 TKT	10908 142 1636 2026 2180 231 2739 2876 5373 5728 5743 5973 6484 6609 7086 847	Homo sapiens (human)
DOID:11504	autonomic neuropathy	ABO ACE ACHE ALDH3A2 ARSA B4GALNT1 BST2 CACNA2D2 CD1D CDH13 CHI3L1 COL9A2 COMT CYB5R3 CYP1A2 CYP27A1 CYP2B6 CYP2C8 CYP2C9 DEGS1 DLD ELOVL4 ENO2 ENPP2 FCN2 GAD1 GAD2 GBA1 GBA2 GCDH GLUL GOLPH3 GPI GPX1 GUSB HK1 HPGDS HPRT1 IDH3A IDS INPPL1 KL L1CAM LYZ MAG MANBA MANEAL MGLL NAGA NCAM1 NCAN NEU3 OGA OGDH PAFAH1B1 PARP1 PGP PIGW PIK3CA PIK3CB PIK3CD PIK3CG PLA2G10 PLA2G2A PLA2G4A PLA2G6 PLB1 PNP PNPLA6 PPT1 PRNP PTEN PTGS2 SARM1 SEMA7A SHMT1 SIGLEC7 SIRT2 SLC2A4 SLC39A8 SMPD1 SMPD3 SMUG1 SPTLC1 ST8SIA4 SUCLA2 TMED9 TPI1	1012 10558 10724 10825 10908 1116 11343 1298 1312 142 1463 149175 151056 1544 1555 1558 1559 1593 1636 1727 1738 2026 2220 224 22933 23098 23583 2571 2572 2583 2629 2639 27036 27306 2752 28 2821 283871 284098 2876 2990 3098 3251 3419 3423 3636 3897 4069 4099 410 4126 43 4668 4684 4860 4967 5048 5168 5290 5291 5293 5294 5320 5321 54732 5538 55512 5621 5728 5743 57704 64083 64116 6470 6517 6609 6785 684 7167 7903 8398 8399 8482 8560 8803 912 9254 9365	Homo sapiens (human)
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	Tlr2 Tlr4	21898 24088	Mus musculus (house mouse)
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	Tl	43222	Drosophila melanogaster (fruit fly)
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	Tlr4	29260	Rattus norvegicus (Norway rat)
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	CAT TLR2 TLR4	7097 7099 847	Homo sapiens (human)
DOID:11507	rumination disorder Aliases: Psychogenic rumination	COMT FUT3 IDS	1312 2525 3423	Homo sapiens (human)
DOID:11512	Budd-Chiari syndrome Aliases: hepatic vein thrombosis	CALR CD55 CYP2C9 GPLD1 PIGM	1559 1604 2822 811 93183	Homo sapiens (human)
DOID:11514	fissured tongue Aliases: Congenital fissure of tongue Congenital plicated tongue Fissure of tongue Fissure of tongue, congenital Furrowed tongue Plicated tongue Tongue, Fissured geographic tongue and fissured tongue lingua plicata scrotal tongue	DHCR7 FCN2 HPGDS PIK3CA PTEN SDHB SDHC SDHD	1717 2220 27306 5290 5728 6390 6391 6392	Homo sapiens (human)
DOID:11516	hypertensive heart disease	ACE CYP11B2 SLC33A1	1585 1636 9197	Homo sapiens (human)
DOID:11527	laryngostenosis Aliases: Stenosis of larynx	FIG4 GLT8D1 SLC26A2	1836 55830 9896	Homo sapiens (human)
DOID:11541	recurrent corneal erosion Aliases: recurrent erosion of cornea recurrent erosion syndrome	ASAH1 B3GALNT2 B3GLCT B4GAT1 CHST6 CRPPA CTNS CTSA CYP1B1 DAG1 FKRP FKTN FUCA1 GLA GLB1 GUSB IDUA KDSR LARGE1 LCAT MYORG NEU1 NGLY1 OCRL PIGL PIGN POMGNT1 POMGNT2 POMK POMT1 POMT2 RXYLT1 SRD5A3 STS SUMF1	10329 10585 11041 145173 148789 1497 1545 1605 2218 23556 2517 2531 2717 2720 285362 2990 29954 3425 3931 412 4166 427 4758 4952 5476 55624 55768 57462 729920 79147 79644 84197 84892 9215 9487	Homo sapiens (human)
DOID:11550	oculomotor nerve paralysis Aliases: III nerve palsy IIIrd nerve Paralysis Third cranial nerve paralysis	ACSM3	6296	Homo sapiens (human)
DOID:11554	Chandler syndrome Aliases: Chandler's syndrome Dystrophy of corneal endothelium Endothelial corneal dystrophy Posterior membrane corneal dystrophy	NEIL1 PIK3CA PIK3CB PIK3CD PIK3CG	5290 5291 5293 5294 79661	Homo sapiens (human)
DOID:11555	Fuchs' endothelial dystrophy Aliases: FCED Fuchs' corneal dystrophy Fuchs' endothelial corneal dystrophy	NEIL1 PIK3CA PIK3CB PIK3CD PIK3CG	5290 5291 5293 5294 79661	Homo sapiens (human)
DOID:1156	chondrocalcinosis Aliases: calcium pyrophosphate deposition disease pseudogout	ACE ALPL ANXA5 CD44 CYP19A1 ENPP1 GALNT3 HSPG2 KL PTGS2	1588 1636 249 2591 308 3339 5167 5743 9365 960	Homo sapiens (human)

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