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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 **7376 - 7400** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:13922	eosinophilic esophagitis	AGA AGXT ALOX15 ALOX5 ANXA5 CD1D CD44 CHIA CLC CLEC16A CYP2C19 ICAM1 IL18R1 IL1RL1 LALBA LCT LTC4S MPG OGDHL PRG2 PTGS2 SGSH SIGLEC8 SOAT1 VCAM1	1178 1557 175 189 23274 240 246 27159 27181 308 3383 3906 3938 4056 4350 5553 55753 5743 6448 6646 7412 8809 912 9173 960	Homo sapiens (human)
DOID:14686	Axenfeld-Rieger syndrome Aliases: Anomaly, Rieger's Axenfeld syndrome RGS - Rieger syndrome Rieger's anomaly	B3GLCT CRPPA CYP1B1 FKRP FKTN LARGE1 POMT1 POMT2 PTGDS	10585 145173 1545 2218 29954 5730 729920 79147 9215	Homo sapiens (human)
DOID:0070255	congenital disorder of glycosylation type IIc Aliases: CDG IIc CDG2C CDGIIc Rambam-Hasharon syndrome	nac	40981	Drosophila melanogaster (fruit fly)
DOID:12930	dilated cardiomyopathy Aliases: primary dilated cardiomyopathy	cs fkrp	322339 571426	Danio rerio (zebrafish)
DOID:1787	pericarditis	CAT LACC1 NT5E PMM2 SMUG1	144811 23583 4907 5373 847	Homo sapiens (human)
DOID:6457	Cowden syndrome Aliases: Cowden disease Lhermitte-Duclos disease dysplastic Gangliocytoma of Cerebellum	ACAN ACAT1 ACE ARSD CEACAM6 CHST3 COL9A2 CYP11A1 DGCR2 GPX1 IL18RAP MBL2 MUTYH PIK3CA PIK3CB PIK3CD PIK3CG PTEN SCD SDC1 SDHB SDHC SDHD SORD	1298 1583 1636 176 2876 38 414 4153 4595 4680 5290 5291 5293 5294 5728 6319 6382 6390 6391 6392 6652 8807 9469 9993	Homo sapiens (human)
DOID:7173	cloacogenic carcinoma Aliases: Cloacogenic anal carcinoma	SMUG1	23583	Homo sapiens (human)
DOID:327	syringomyelia	CD38 CNTN2 CYP2U1 ERLEC1 GNPTAB HPRT1 IL18RAP PTGS2 SMUG1 TMTC1	113612 23583 27248 3251 5743 6900 79158 83857 8807 952	Homo sapiens (human)
DOID:0050730	coenzyme Q10 deficiency disease Aliases: COENZYME Q10 DEFICIENCY, PRIMARY	Coq2	498332	Rattus norvegicus (Norway rat)
DOID:0060319	cardiac arrest Aliases: cardiopulmonary arrest circulatory arrest	Tnf	21926	Mus musculus (house mouse)
DOID:0080556	congenital disorder of glycosylation Id Aliases: congenital disorder of glycosylation 1d	Alg3	287983	Rattus norvegicus (Norway rat)
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	ZWF1	855480	Saccharomyces cerevisiae S288C
DOID:13276	Mycoplasma pneumoniae pneumonia Aliases: Mycoplasma pneumonia Mycoplasmal pneumonia Pneumonia due to Eaton's agent Pneumonia due to Mycoplasma pneumoniae Pneumonia due to Mycoplasma pneumoniae (disorder) cold agglutinin positive pneumonia	ACE CLEC5A CYP1A1 GALC SELE TNF	1543 1636 23601 2581 6401 7124	Homo sapiens (human)
DOID:12783	migraine without aura Aliases: common migraine	Eno	33351	Drosophila melanogaster (fruit fly)
DOID:3594	choriocarcinoma Aliases: Chorioepithelioma	Igf2	24483	Rattus norvegicus (Norway rat)
DOID:2033	communication disorder	ARSD DLD GPD2 PPP1R3A PRPS1 PTEN STS	1738 2820 412 414 5506 5631 5728	Homo sapiens (human)
DOID:2739	Gilbert syndrome Aliases: Constitutional hyperbilirubinemia Gilbert's disease Gilbert's syndrome Gilbert-Meulengracht syndrome hereditary nonhemolytic jaundice	ugt1a1 ugt1a6	100135191 100489505	Xenopus tropicalis (tropical clawed frog)
DOID:106	pleural tuberculosis Aliases: Pearly disease Tuberculosis of pleura Tuberculous pleurisy Tuberculous pleuritis tuberculous pleurisy in primary progressive tuberculosis	Tl	43222	Drosophila melanogaster (fruit fly)
DOID:12451	sulfhemoglobinemia	APRT CYB5R3 CYP1A2 DLD G6PC1 G6PD	1544 1727 1738 2538 2539 353	Homo sapiens (human)
DOID:0060076	estrogen-receptor negative breast cancer	CBR1	854768	Saccharomyces cerevisiae S288C
DOID:3083	chronic obstructive pulmonary disease Aliases: COLD COPD chronic obstructive airway disease chronic obstructive lung disease	ACE ACHE ACLY ACOT7 ACSS2 ADIPOQ AGPAT3 ALDH2 ALOX15 ALPI ALPP ANXA5 ARSA ARSB C1GALT1 CALR CAT CD14 CD1D CD33 CD38 CD74 CDH13 CEACAM5 CEL CH25H CHI3L1 CHIT1 CLEC7A CNTN4 COMT CS CYP1A1 CYP1A2 CYP1B1 CYP2B6 CYP2E1 CYP3A5 CYP7B1 DCN DHCR24 EPHX2 FDPS FUT8 GAD1 GALC GALNS GALNT13 GLA GLB1 GM2A GPX1 GPX3 HAS2 HPGDS HSD11B1 HSD17B6 HTR2A HYAL1 ICAM1 IDS IL18R1 IL1RAP IL1RL1 INPP5D ISYNA1 ITPK1 KL KLRK1 LAYN LEP LEPR LGALS3 LGALS9 LTC4S MBL2 MRC1 NT5E NTM OGG1 PARP1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G10 PLA2G15 PLA2G1B PLA2G2A PLA2G2D PLA2G4C PLAUR PLB1 PLCE1 POFUT1 PPARGC1A PRNP PTEN PTGDS PTGS1 PTGS2 RECK SARM1 SDC4 SDHB SELL SELP SFTPA1 SFTPA2 SFTPC SFTPD SGPL1 SGSH SIGLEC8 SIGLEC9 SIRT2 SIRT6 SLC27A5 SLC2A4 SLC35F3 SMPD1 SMPD3 SMUG1 SOAT1 SORD SPAM1 SPHK1 STS SUMF1 TLR4 TM7SF2 TNF TNFRSF10C UGCG VCAN	1012 1048 1056 10891 10998 1116 1118 11332 114805 1312 142 1431 143903 1462 148641 151056 152330 1543 1544 1545 1555 1571 1577 1634 1636 1718 2053 217 2224 22914 22933 23098 23509 23583 23659 246 248 250 2530 2571 2581 2588 26279 2717 27180 27181 2720 27306 2760 285362 2876 2878 3037 308 3290 3356 3373 3383 3423 3556 3635 3705 3952 3953 3958 3965 4056 410 411 412 4153 43 4360 47 4907 4968 50863 51196 51477 51548 5290 5291 5293 5294 5319 5320 5329 55512 55902 5621 56894 56913 5728 5730 5742 5743 6385 6390 6402 6403 6440 6441 6448 64581 6517 653509 6609 6646 6652 6677 7099 7108 7124 729238 7357 811 83666 8399 8434 847 8605 8630 8794 8809 8877 8879 9023 912 9173 929 9365 9370 9420 945 952 972	Homo sapiens (human)
DOID:12712	nephronophthisis Aliases: medullary cystic disease medullary cystic kidney	ACE AGXT ALDH3A2 LGALS1 MLYCD UMOD	1636 189 224 23417 3956 7369	Homo sapiens (human)
DOID:0070331	mitochondrial DNA depletion syndrome 8b Aliases: mitochondrial neurogastrointestinal encephalopathy syndrome, RRM2B-related	TYMP	1890	Homo sapiens (human)
DOID:0080055	achondrogenesis type IB Aliases: achondrogenesis Fraccaro type	DCN SLC26A2	1634 1836	Homo sapiens (human)
DOID:0111352	D-2-hydroxyglutaric aciduria 2 Aliases: D2HGA2	IDH2	3418	Homo sapiens (human)

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