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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 **6201 - 6225** of **7942** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism
DOID:4029	gastritis Aliases: Erosive Gastritis Erosive gastropathy acute gastric mucosal erosion	A4GNT ACE CAT CD177 CD44 CHIT1 CYP2C19 CYP2C9 FCER2 FCGR3B FUT2 FUT4 HPGDS ICAM1 IL18R1 LCT LGALS1 LYZ MDH2 NT5E PLCE1 PTGDS PTGS1 PTGS2 SELE SELL SIGLEC8 SIRT2 SMUG1 TNF UGT1A6 VTCN1	1118 1557 1559 1636 2208 2215 22933 23583 2524 2526 27181 27306 3383 3938 3956 4069 4191 4907 51146 51196 54578 57126 5730 5742 5743 6401 6402 7124 79679 847 8809 960	Homo sapiens (human)
DOID:403	mouth disease	PTGS2	5743	Homo sapiens (human)
DOID:4030	eosinophilic gastritis	SIGLEC8	27181	Homo sapiens (human)
DOID:4031	eosinophilic gastroenteritis	SIGLEC8	27181	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:4051	alveolar rhabdomyosarcoma Aliases: alveolar childhood rhabdomyosarcoma	CPT1A NCAM1 PIK3CA SGPL1 SLC2A4 SMUG1	1374 23583 4684 5290 6517 8879	Homo sapiens (human)
DOID:4051	alveolar rhabdomyosarcoma Aliases: alveolar childhood rhabdomyosarcoma	foxo1a	768121	Danio rerio (zebrafish)
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:4074	pancreatic adenocarcinoma Aliases: pancreas adenocarcinoma	ACSS2 AGPAT2 AKR1A1 AKR1B10 ALOX5 ALPI ALPP ARSA CAT CD109 CD44 CEACAM5 CEACAM6 CEACAM7 CYP1A1 CYP1A2 DCTD DPEP1 GAPDH GPC1 HMMR HPGDS HPSE ICAM1 IL1RAP IL1RL1 KL L1CAM LGALS3 LGALS4 MRC1 MSLN MTAP NTHL1 PDHX PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PLPP5 PNP PTEN PTGS2 SDC1 SDC2 SDHB SELL SFTPD SMUG1 ST3GAL3 ST3GAL4 STS THEM4 TM7SF2 UGT1A7	10232 10327 1048 10555 10855 1087 117145 135228 1543 1544 1635 1800 23583 23659 240 248 250 2597 27306 2817 3161 3383 3556 3897 3958 3960 410 412 4360 4507 4680 4860 4913 5290 5291 5293 5294 54577 55902 57016 5728 5743 6382 6383 6390 6402 6441 6484 6487 7108 8050 84513 847 9173 9365 960	Homo sapiens (human)
DOID:4078	tricuspid valve stenosis Aliases: Tricuspid stenosis	CHST3 HEXD OGA	10724 284004 9469	Homo sapiens (human)
DOID:4079	heart valve disease Aliases: Valvular heart disease	Galnt1 Tnf	24835 79214	Rattus norvegicus (Norway rat)
DOID:4079	heart valve disease Aliases: Valvular heart disease	Galnt1 Lrp5 Tnf	14423 16973 21926	Mus musculus (house mouse)
DOID:4079	heart valve disease Aliases: Valvular heart disease	gly-3	176112	Caenorhabditis elegans
DOID:4079	heart valve disease Aliases: Valvular heart disease	galnt1	559073	Danio rerio (zebrafish)
DOID:4079	heart valve disease Aliases: Valvular heart disease	Pgant5	326151	Drosophila melanogaster (fruit fly)
DOID:4079	heart valve disease Aliases: Valvular heart disease	galnt1	594943	Xenopus tropicalis (tropical clawed frog)
DOID:4079	heart valve disease Aliases: Valvular heart disease	ACACA ACE CALR FDPS GALNT1 IDS IL1R1 LRP5 TNF	1636 2224 2589 31 3423 3554 4041 7124 811	Homo sapiens (human)
DOID:4080	tricuspid valve insufficiency Aliases: Tricuspid incompetence Tricuspid regurgitation Tricuspid valve regurgitation	CHST3 HADHA HADHB PLD1 PTGS2 SDHD	3030 3032 5337 5743 6392 9469	Homo sapiens (human)
DOID:4085	trophoblastic neoplasm Aliases: Trophoblastic tumor	HSD3B1 LGALS1	3283 3956	Homo sapiens (human)
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	Tnf	21926	Mus musculus (house mouse)
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	GTB1	851807	Saccharomyces cerevisiae S288C
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	ACACA ACADM ACADVL ACE ACHE ACOT7 ADH1A ADH1B ADH1C AKR1A1 AKR1B10 AKR1C1 AKR1D1 ALDH1B1 ALDH2 ALPP AMACR ARSH ASAH2 ATP6AP1 ATP6AP2 ATRNL1 CCDC115 CD14 CD1D CD209 CEACAM5 CEACAM7 CFC1 CHI3L1 CLEC1B COMT CYP17A1 CYP1A1 CYP1A2 CYP1B1 CYP2B6 CYP2C19 CYP2C9 CYP2E1 CYP3A4 CYP4F3 CYP51A1 CYP7A1 CYP7B1 DLAT EHHADH ENO3 ENPP2 EXT1 FUT1 FUT2 G6PC1 GALT GANAB GBE1 GGT1 GLO1 GLUL GOLPH3 GP2 GPC3 GUSB H6PD HADH HADHA HAS1 HAS3 HK3 HMGCS2 HPGDS HSD11B1 HSD17B6 HSD3B7 ICAM1 IGF2R IL1RAP IMPA1 ISYNA1 KDSR KLRK1 LCAT LGALS3 LGALS9 LIPA LYZ MAN1B1 MASP1 MBL2 MBOAT7 MICA MPI MTAP NAGA NAMPT NCAM1 NEIL1 NTM OGG1 OLR1 OPCML PEMT PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G5 PMM2 PNPLA3 POFUT1 PRKAA2 PRKCSH PTEN PTGS2 RENBP RGN SC5D SDC1 SELP SIGLEC7 SIRT6 SLC17A5 SLC35A2 SMUG1 SPHK2 SRD5A2 ST3GAL4 ST6GAL1 ST8SIA1 ST8SIA4 STS SULT1E1 TALDO1 TKFC TKT TM7SF2 TMEM199 TNF UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B7 UMOD VCAM1 XYLT2	100507436 10135 10159 10327 10400 1048 1087 1116 11253 11332 124 125 126 1312 147007 1543 1544 1545 1555 1557 1559 1571 1576 1581 1586 1595 1636 1645 1737 1962 2027 2131 217 219 22914 23193 23509 23583 23600 250 2523 2524 2531 2538 2592 26007 26033 2632 26503 2678 27036 2719 27306 2739 2752 2813 2990 3030 3033 3036 3038 30835 31 3101 3158 3290 3383 34 347527 3482 3556 3612 37 3931 3958 3965 3988 4051 4069 412 4153 43 4351 4507 4668 4684 4968 4973 4978 50863 51266 51477 51548 5168 5290 5291 5293 5294 5315 5322 537 5373 54575 54576 54577 54578 54579 54600 54657 54658 54659 5563 5589 55997 5648 56624 56848 56886 57016 5728 5743 5973 6309 6382 6403 64083 64132 6480 6484 6489 6716 6718 6783 6888 7086 7108 7124 7355 7364 7369 7412 7903 79143 79661 80270 80339 84317 8630 9104 912 929 9420 9563	Homo sapiens (human)
DOID:409	liver disease Aliases: disorder of liver hepatic disorder	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:4090	agnosia Aliases: Dyspraxia Dyspraxia syndrome	ACADSB ACAT1 ACE AGK AGRN ALDH2 ALDH5A1 ALG13 ALG14 ALG2 ARSA ASAH1 ATP6AP2 ATP6V0A2 ATP6V1A B3GALNT2 B3GAT1 CACNA2D2 CAT CHAT CHI3L1 CHKB CHST14 CHST3 CLN5 COG4 COG5 COMT CRPPA CYP19A1 CYP27B1 CYP2B6 CYP2C9 CYP2R1 CYP2U1 CYP3A4 CYP3A5 DAG1 DGKK DPAGT1 EPM2A EXT2 EXTL3 FASN FCGR3B FKRP FKTN GAD2 GALT GBA1 GCK GFPT1 GMDS GMPPB GPAA1 GPX1 GPX3 HACD1 HADH HADHA HADHB HGSNAT HIBCH HPRT1 INPP5K LARGE1 LGALS1 LMAN2L MAN1B1 MBOAT7 MDH2 MGLL MTMR14 MTMR2 NDST1 PGAP1 PIGC PIK3CA PLA2G6 PLCB4 PNP PNPLA2 POMGNT1 POMK POMT1 POMT2 PRNP PRPS1 PSAP PTEN PTGS2 RPIA SDHA SDHB SDHD SLC35G1 SRD5A3 ST3GAL3 ST3GAL5 TECR TUSC3 UGT2B7	10159 10466 10585 1103 1116 1120 11253 113189 11343 113612 120227 1203 1312 138050 139189 148789 1555 1559 1576 1577 1588 159371 1594 1605 1636 1798 199857 2132 2137 217 2194 2215 2218 22934 23545 2572 25839 2592 26275 2629 2645 2673 27087 2762 2876 2878 29925 29954 3030 3032 3033 3251 3340 36 375790 38 3956 410 4191 427 4860 51763 523 5279 5290 5332 55624 55750 5621 5631 5660 57104 5728 5743 6389 6390 6392 64419 6487 729920 7364 79143 79147 7915 7957 79644 79868 7991 80055 81562 8398 84197 847 85365 8733 8869 8898 9200 9215 9254 9469 9524	Homo sapiens (human)
DOID:4131	erythrasma Aliases: Infection due to Corynebacterium minutissimum	CAT	847	Homo sapiens (human)

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