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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **2476 - 2500** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼
DOID:2951	motion sickness Aliases: Travel Sickness	GPD2	2820	Homo sapiens (human)
DOID:9253	gastrointestinal stromal tumor Aliases: GANT GIST Stromal tumor of gastrointestinal tract Stromal tumour of gastrointestinal tract gastrointestinal stromal tumour	ALDH7A1 AMACR ANXA5 CD14 CD44 CD55 CMAS CYP1A2 CYP1B1 CYP2C8 EPHX2 FASN HSD11B1 L1CAM LDHA LYZ MCAT MGLL MTAP NCAM1 NDST1 PIK3C2A PIK3CA PIK3CB PIK3CD PIK3CG PKM PLCB4 PTEN PTGS2 SDHA SDHB SDHC SDHD SELP SLC2A4 SMUG1 SOAT1 SORD TKTL1 VCAN	11343 1462 1544 1545 1558 1604 2053 2194 23583 23600 27349 308 3290 3340 3897 3939 4069 4507 4684 501 5286 5290 5291 5293 5294 5315 5332 55907 5728 5743 6389 6390 6391 6392 6403 6517 6646 6652 8277 929 960	Homo sapiens (human)
DOID:707	B-cell lymphoma Aliases: B-cell lymphocytic neoplasm	ACAA1 ACACA ACACB ACE ACHE ACSBG1 ACSF3 AKR1A1 AKR1C1 AKR1C3 ALG1 ALPP AMACR ANXA5 APRT ATRNL1 CAT CD14 CD22 CD33 CD38 CD44 CD55 CD74 CDH13 CDS1 CEACAM5 CEL CFC1 CHI3L1 CLEC10A CNTN2 COMT CS CSPG4 CYP17A1 CYP1A1 CYP1B1 CYP24A1 CYP27B1 CYP2B6 CYP2C9 CYP2E1 EPHX2 FASN FBP1 FCER2 FCGR3B FCN2 FH FMOD FUT1 G6PD GAPDH GBA1 GBE1 GFRA1 GGT1 GLB1 GLDC GPX1 H6PD HACD1 HK2 HPGDS HYAL2 ICAM1 IDH1 IDH2 IL1R1 IL1RAPL1 INPP5D ITPKB KDSR KL KLRK1 LDHA LGALS1 LGALS3 LY6G6D LYPD5 MASP2 MCAT MRC1 MTAP NAMPT NCAM1 NTHL1 OGG1 PAFAH1B1 PARP1 PARP9 PC PDHX PIK3CA PIK3CB PIK3CD PIK3CG PIKFYVE PKM PRKAA2 PSMD10 PTEN PTGS2 SDC1 SELE SELL SHMT1 SHMT2 SIGLEC10 SIRT4 SLC27A5 SLC2A2 SLC2A3 SLC2A4 SLC35B2 SMUG1 SOAT1 SPHK1 STS TMEM260 VCAM1 VNN1 VTCN1	1012 10135 10327 1040 10462 1048 1056 10747 10998 11141 1116 1312 142 1431 1464 1543 1545 1555 1559 1571 1586 1591 1594 1604 1636 1645 197322 200576 2053 2194 2203 2208 2215 2220 2271 22914 23205 2331 23409 23583 23600 250 2523 2531 2539 2597 26033 2629 2632 2674 2678 2720 27306 2731 27349 284348 2876 30 308 3099 31 32 3383 3417 3418 347734 353 3554 3635 3707 3939 3956 3958 412 43 4360 4507 4684 4913 4968 5048 5091 5290 5291 5293 5294 5315 54916 5563 55997 56052 5716 5728 5743 58530 6382 6401 6402 6470 6472 6514 6515 6517 6646 6900 7412 79679 8050 83666 847 8644 8692 8876 8877 89790 9200 929 933 9365 945 952 9563 960 972	Homo sapiens (human)
DOID:8619	recurrent hypersomnia Aliases: primary recurrent hypersomnia	ABAT CD55 CHKB COMT HACD1 LGALS3 PNPLA6 PRNP SMUG1	10908 1120 1312 1604 18 23583 3958 5621 9200	Homo sapiens (human)
DOID:0111633	congenital sucrase-isomaltase deficiency Aliases: CSID SI deficiency congenital sucrase-isomaltose malabsorption congenital sucrose intolerance disaccharide intolerance	SI	6476	Homo sapiens (human)
DOID:769	neuroblastoma	AACS ACADM ACAT1 ACHE ACO1 ADH1A AKR1B1 ALDH1A3 ALDOC ALOX12 ALOX5 ALPI ALPP AMACR ANXA5 APRT ARSA ARSF ARSH ASAH2 B3GAT1 B3GNT3 B4GALNT1 B4GALT3 CALR CAT CCDC115 CD14 CD177 CD1D CD248 CD38 CD44 CD55 CDH13 CEACAM5 CERK CERS1 CFC1 CHAT CHGA CHKA CHPT1 COMT CS CYP19A1 CYP3A4 CYP3A5 DCN DGCR2 DHCR24 DHDDS DLD EBP ENO1 ENO2 ENPP2 EXTL1 FCGR3B FCN2 FH FIG4 G6PC1 G6PD GAD1 GALNT14 GALNT9 GAPDH GAS1 GBA1 GCNT1 GDPD5 GFRA2 GLB1 GLDC GOLPH3 GPC2 GPC3 GPX1 GUSB HAS3 HK2 HPGDS HPRT1 HPSE HSD17B12 HSD17B6 ICAM1 ICAM2 IL18R1 ITLN1 KLRK1 L1CAM LDHA LDHB LDHC LGALS1 LGALS3 LGALS4 LMAN2 LYPD5 MAG MCAT MGAT2 MGAT5 MGAT5B MGLL MICA MMUT MRC1 MTAP NAGLU NAMPT NANS NCAM1 NCAN NEU4 NT5E OGDH PARP1 PARP2 PARP3 PDIA3 PFKFB3 PGK1 PGP PIK3C2B PIK3C2G PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLB1 PLCB1 PNP PNPLA6 POMGNT1 PPT1 PPT2 PRKAA2 PRNP PRPS1 PTEN PTGES PTGS2 QPRT RECK RENBP RTN4R SDC1 SDHA SDHB SDHC SDHD SELE SELP SHMT2 SIGLEC7 SIRT4 SIRT6 SLC2A3 SLC2A5 SLC39A8 SMUG1 SOAT1 SORD SPHK2 ST8SIA1 ST8SIA2 ST8SIA4 SUCLA2 SULF2 SYNJ1 TNFRSF10C TNKS TPI1 TYMP VCAM1 VCAN	10038 10039 100507436 1012 10135 10331 1048 10682 10715 10855 10908 10960 1103 1113 1119 11343 124 129807 1312 142 1431 1462 1463 146664 151056 1576 1577 1588 1604 1634 1718 1738 1890 2023 2026 2134 220 2215 221914 2220 2271 22914 230 231 23236 23409 23475 23583 23600 239 240 248 250 2538 2539 2571 2583 2597 2619 2629 2650 2675 27036 27087 2719 2720 27306 2731 27349 283871 284348 2876 2923 2990 3038 308 3099 3251 3383 3384 34 347527 353 38 3897 3939 3945 3948 3956 3958 3960 4099 410 416 4247 4249 43 4360 4507 4594 4669 4684 48 4860 4907 4967 50614 51144 51548 5168 5209 5230 5287 5288 5290 5291 5293 5294 5319 5320 5321 54187 5538 55600 55624 5563 55959 55997 5621 5631 56624 56848 56994 57124 57126 5728 5743 5973 6382 6389 6390 6391 6392 6401 6403 64083 64116 6472 64781 6489 65078 6515 6518 65985 6646 6652 7167 7412 7903 79623 79947 811 8128 81544 8398 84317 8434 847 8630 8658 8703 8794 8803 8809 8867 912 929 9374 952 9536 960 9896 9993	Homo sapiens (human)
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)
DOID:13364	obsolete chronobiology disease	ACE	1636	Homo sapiens (human)
DOID:0060648	anterior segment dysgenesis Aliases: anterior segment developmental anomaly corneal opacification and other ocular anomalies sclerocornea with other ocular anomalies	CYP1B1	1545	Homo sapiens (human)
DOID:10146	thymus lymphoma	MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN	4360 5290 5291 5293 5294 5728	Homo sapiens (human)
DOID:4045	muscle cancer Aliases: malignant neoplasm of muscle malignant tumor of muscle malignant tumor of the Muscle myosarcoma	CDH13 FH	1012 2271	Homo sapiens (human)
DOID:0060847	Leri-Weill dyschondrosteosis	EXT1 EXT2	2131 2132	Homo sapiens (human)
DOID:13088	periventricular leukomalacia	ACE ECHS1 EOGT PC PLA2G6 PMM2 SFTPD TNF TPI1	1636 1892 285203 5091 5373 6441 7124 7167 8398	Homo sapiens (human)
DOID:0090081	hypogonadotropic hypogonadism 22 with or without anosmia	ACSM3 ADH5 CD44 CD55 CYP17A1 CYP19A1 GAS1 GK GPC1 HJV HS6ST1 HSD17B3 L1CAM MMUT NT5E PMM2 PNPLA6 SEMA7A SMPD3 SOAT1 STS TYMP	10908 128 148738 1586 1588 1604 1890 2619 2710 2817 3293 3897 412 4594 4907 5373 55512 6296 6646 8482 9394 960	Homo sapiens (human)
DOID:0060427	chromosome Xp21 deletion syndrome Aliases: Xp21 microdeletion syndrome complex glycerol kinase deficiency monosomy Xp21	GK IL1RAPL1	11141 2710	Homo sapiens (human)
DOID:2365	West Nile encephalitis Aliases: West Nile Fever with encephalitis West Nile fever encephalitis	NAMPT PIK3CA PIK3CB PIK3CD	10135 5290 5291 5293	Homo sapiens (human)
DOID:1993	rectum cancer Aliases: carcinoma of rectum carcinoma of the rectum malignant Rectal tumor malignant neoplasm of rectum malignant rectum tumor malignant tumor of rectum rectal cancer	ABO ACAT1 ACE ACSS2 ALDH2 ALDH7A1 ALDOB ALOX12 ALOX15 ARSA ASAH1 CALR CD44 CEACAM5 CEACAM7 CERS4 CERS5 CHI3L1 CHPT1 COMT CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP24A1 CYP2E1 DHCR24 DHDDS EXT1 FH GPX2 GPX3 HMGCS2 HPGDS HSD17B2 MAPK14 MICA MRC1 MUTYH NT5E NTHL1 OGG1 PARP1 PCK2 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PLA2G4A PNPLA2 PTEN PTGS1 PTGS2 RENBP SDHA SDHC SMUG1 TDG TKT TKTL1 TYMP UGT1A1 UMPS	100507436 1048 1087 1116 1312 142 1432 1543 1544 1571 1586 1588 1591 1636 1718 1890 2131 217 2271 229 23583 23659 239 246 27306 28 2877 2878 3158 3294 38 410 427 4360 4595 4907 4913 4968 501 5106 5290 5291 5293 5294 5321 54658 55902 56994 57104 5728 5742 5743 5973 6389 6391 6996 7086 7372 79603 79947 811 8277 91012 960	Homo sapiens (human)
DOID:10591	pre-eclampsia Aliases: gestational hypertension hypertension induced by pregnancy pre-eclamptic toxaemia preeclampsia preeclampsia/eclampsia pregnancy associated hypertension pregnancy toxemia proteinuric hypertension of pregnancy toxaemia of pregnancy	ACE ACOT7 AKR1C3 ANXA5 ATP6AP2 CALR CHI3L1 COMT CYP11B1 CYP11B2 CYP19A1 CYP21A2 CYP24A1 CYP27B1 CYP2J2 CYP2R1 CYP3A5 EFNA1 ENPP1 GAPDH GPI GPX1 GPX3 HADHA HPGDS HSD11B1 HSD11B2 HSD3B1 HSD3B2 HSPG2 ICAM1 IL18R1 ISYNA1 LEP LEPR LGALS1 LIPC LPL MBL2 OGG1 OLR1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PLA2G6 PLAUR PLB1 PTGDS PTGS1 PTGS2 PYGM RBP4 RENBP SDC1 SELL SIRT4 SLC17A5 SLC2A1 TLR4 TNF VCAM1	10159 1116 11332 120227 1312 151056 1573 1577 1584 1585 1588 1589 1591 1594 1636 1942 23409 2597 26503 27306 2821 2876 2878 3030 308 3283 3284 3290 3291 3339 3383 3952 3953 3956 3990 4023 4153 4968 4973 51477 5167 5290 5291 5293 5294 5320 5329 5730 5742 5743 5837 5950 5973 6382 6402 6513 7099 7124 7412 811 8398 8644 8809	Homo sapiens (human)
DOID:0050211	swine influenza	PIK3CG	5294	Homo sapiens (human)
DOID:8850	salivary gland cancer Aliases: malignant neoplasm of salivary gland	ACACB ISYNA1 LGALS3 MSLN PYGB ST3GAL4 VCAN	10232 1462 32 3958 51477 5834 6484	Homo sapiens (human)
DOID:0050460	Wolf-Hirschhorn syndrome Aliases: 4p deletion syndrome PITT SYNDROME Pitt-Rogers-Danks Syndrome chromosome 4p16.3 deletion syndrome	IL1RL1	9173	Homo sapiens (human)
DOID:0111405	Fraser syndrome 1 Aliases: FRASRS1	FREM1 NT5E	158326 4907	Homo sapiens (human)
DOID:12705	Friedreich ataxia Aliases: Friedreich's ataxia Friedreich's tabes	ACO2 CAT COG5 DLD GAA GPAA1 GPX1 HPGDS HSD17B4 ICAM1 LPL PIP5K1B PRKAA2 PRNP PTGS2 VCAM1	10466 1738 2548 27306 2876 3295 3383 4023 50 5563 5621 5743 7412 8395 847 8733	Homo sapiens (human)
DOID:1063	interstitial nephritis Aliases: renal tubulo-interstitial disease	ACE APRT CAT CYP2C9 DCN DHCR7 DPEP1 GLA HSPG2 IL18R1 MMUT PLA2R1 REG3G SDC1 SDC2 SFTPA1 SFTPA2 SFTPD SLC3A1 TM7SF2 UMOD	130120 1559 1634 1636 1717 1800 22925 2717 3339 353 4594 6382 6383 6441 6519 653509 7108 729238 7369 847 8809	Homo sapiens (human)
DOID:3490	Noonan syndrome Aliases: Turner's phenotype, karyotype normal	ACADS AMT ARSA ARSD B4GALT7 BAAT CAT CHPT1 CYP11A1 DAG1 DCN DHDDS 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 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)

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