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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 **576 - 600** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:8649	tongue cancer Aliases: malignant neoplasm of tongue	CALR DAG1 GOLPH3 HPSE KLRC1 LGALS3 LSS NANS PIK3CA PIK3CB PIK3CD PIK3CG PLAUR PTEN PTGS2	10855 1605 3821 3958 4047 5290 5291 5293 5294 5329 54187 5728 5743 64083 811	Homo sapiens (human)
DOID:0070433	hyperphosphatasia with impaired intellectual development syndrome 1 Aliases: GPIBD2 HPMRS1 glycosylphosphatidylinositol biosynthesis defect 2 hyperphosphatasia with mental retardation syndrome 1	pigv-1	172305	Caenorhabditis elegans
DOID:3223	complex regional pain syndrome Aliases: Complex regional pain syndromes	B3GAT1 IL1R1	27087 3554	Homo sapiens (human)
DOID:2988	antiphospholipid syndrome Aliases: APS antiphospholipid antibody syndrome	ANXA5 CALR CD1D GPI IDS LCT LGALS9 MBL2 PC SELP	2821 308 3423 3938 3965 4153 5091 6403 811 912	Homo sapiens (human)
DOID:0111063	hyperphosphatemic familial tumoral calcinosis Aliases: HFTC HHS PHPTC cortical hyperostosis with hyperphosphatemia familial Teutschlaender disease familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome hypercalcemic tumoral calcinosis hyperostosis with hyperphosphatemia hyperphosphatemia hyperostosis hyperphosphatemia hyperostosis syndrome hyperphosphatemia tumoral calcinosis lipocalcinogranulomatosis morbus Teutschlaender primary hyperphosphatemic tumoral calcinosis tumoral calcinosis with hyperphosphatemia	Galnt3 Kl	366061 83504	Rattus norvegicus (Norway rat)
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)
DOID:6725	spinal stenosis Aliases: Spinal stenosis of lumbar region cervical spinal stenosis lumbar spinal stenosis	CAT COL9A2 GOLPH3 LSS PTGS2	1298 4047 5743 64083 847	Homo sapiens (human)
DOID:0110777	hereditary spastic paraplegia 26 Aliases: GM2 synthase deficiency SPG26 autosomal recessive spastic paraplegia 26 autosomal recessive spastic paraplegia type 26	b4galnt1	100145208	Xenopus tropicalis (tropical clawed frog)
DOID:7148	rheumatoid arthritis Aliases: Arthritis or polyarthritis, rheumatic atrophic Arthritis	Chi3l1 Igf2 Pgf Pik3r1 Tnf	24483 24835 25513 89824 94203	Rattus norvegicus (Norway rat)
DOID:0080611	anterior segment dysgenesis 6	CYP1B1	1545	Homo sapiens (human)
DOID:0112222	developmental and epileptic encephalopathy 88 Aliases: DEE88 early infantile epileptic encephalopathy 88	Mdh1	17449	Mus musculus (house mouse)
DOID:9307	rectal prolapse Aliases: Procidentia, rectum	FREM1 PTEN	158326 5728	Homo sapiens (human)
DOID:0080119	mitochondrial DNA depletion syndrome 1 Aliases: mitochondrial DNA depletion syndrome 1 (MNGIE type) mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related	Tymp	315219	Rattus norvegicus (Norway rat)
DOID:8557	oropharynx cancer Aliases: Oropharyngeal carcinoma malignant Oropharyngeal tumor malignant tumor of oropharynx malignant tumour of mesopharynx oropharyngeal cancer	ADH1B ADH1C ADH5 ALDH2 CD44 MTAP NEIL2 PIK3CA PIK3CB PIK3CD PIK3CG SMUG1 TYMP	125 126 128 1890 217 23583 252969 4507 5290 5291 5293 5294 960	Homo sapiens (human)
DOID:7926	epithelial malignant thymoma Aliases: Squamoid Thymoma Thymoma, epithelial Well differentiated thymic carcinoma	LY75	4065	Homo sapiens (human)
DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L Aliases: LGMD2L muscular dystrophy, limb-girdle, type 2L	fktn.S	495324	Xenopus laevis (African clawed frog)
DOID:14221	abdominal obesity-metabolic syndrome 1 Aliases: dysmetabolic syndrome X metabolic syndrome X	Lep	25608	Rattus norvegicus (Norway rat)
DOID:2377	multiple sclerosis Aliases: Generalized multiple sclerosis insular sclerosis	ABO ACAN ACE ACHE ACO2 ACOT7 ADIPOQ AGA AKR1B1 ALOX15 ALOX5 AMACR AMT ANXA5 APRT ARSA ARSF ATP6AP2 B3GAT1 B4GALT5 B4GALT6 BST2 CANX CAT CD14 CD177 CD1D CD38 CD44 CD48 CD74 CEACAM5 CEACAM7 CEMIP CERS2 CERS6 CH25H CHAT CHGA CHI3L1 CHIT1 CLEC12A CLEC16A CLEC4E CNTN1 COLEC12 COMT CPT1A CSGALNACT1 CSGALNACT2 CYP17A1 CYP1B1 CYP21A2 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C9 CYP2R1 CYP3A4 CYP46A1 CYP7A1 CYP7B1 DCN DHCR24 DHCR7 DHRS11 DLD ENO1 ENPP2 FCGR3B FH FOLR2 GAD1 GAD2 GALC GANAB GAPDH GBE1 GLA GLO1 GPC5 GPI H6PD HPGDS HPRT1 HPSE HSD17B6 HSD17B7 ICAM1 ICAM5 IGF2 IL18R1 INPP4B ISYNA1 ITLN1 KL KLRB1 KLRC1 KLRD1 KLRK1 LALBA LDHA LGALS1 LGALS3 LGALS8 LGALS9 LPL MAG MANBA MASP1 MASP2 MBL2 MGAT1 MGAT5 MICA MMP25 MOGAT1 NCAM1 NCAN NT5E OGG1 OLR1 PARP1 PC PCK1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLB1 PLD1 PPT2 PRNP PSMD10 PTGES PTGS2 QTRT1 RGMA RGMB RTN4R SDC1 SELE SELP SEMA7A SGPL1 SHMT1 SIGLEC1 SIRT2 SLC2A4 SMPD1 SOAT1 SPHK1 SPHK2 ST8SIA1 SUMF1 TALDO1 TKT TLR4 TMED5 TNF TNFRSF10C TPI1 VCAM1	100507436 10159 1048 10747 10855 10858 1087 1103 1113 1116 1118 11332 116255 120227 1272 1312 1374 142 1463 151056 1545 1555 1557 1559 1576 1581 1586 1589 1591 1593 1594 160364 1634 1636 1717 1718 1738 175 176 2023 2215 2262 2271 22914 22933 231 23193 23274 2350 23600 240 246 253782 2571 2572 2581 2597 26253 2632 27087 2717 27306 2739 275 28 2821 285362 285704 29956 308 3251 3383 3481 353 3820 3821 3824 3906 3939 3956 3958 3964 3965 4023 4099 410 4126 4153 416 4245 4249 43 4684 4907 4968 4973 50 5091 50999 5105 51477 51478 5168 5290 5291 5293 5294 5319 5320 5321 5337 55454 55600 55790 5621 5648 56848 56963 57126 5716 57214 5743 6382 6401 6403 64386 6470 6489 65078 6517 6609 6614 6646 684 6888 7086 7087 7099 7124 7167 7412 79154 7941 81035 81890 821 8398 847 8482 8630 8794 8809 8821 8877 8879 9023 912 929 9331 9334 9365 9370 9374 9420 952 9536 9563 960 962 972	Homo sapiens (human)
DOID:13507	trigonitis	CAT IMPA1 MBL2 NAGLU OGA PIK3CA PIK3CB PIK3CD PIK3CG PRKAA2 PTGS2	10724 3612 4153 4669 5290 5291 5293 5294 5563 5743 847	Homo sapiens (human)
DOID:9352	type 2 diabetes mellitus Aliases: NIDDM insulin resistance non-insulin-dependent diabetes mellitus type 2 diabetes type II diabetes mellitus	ins.L ins.S	378695 378696	Xenopus laevis (African clawed frog)
DOID:3301	gonadoblastoma	CAT PGD	5226 847	Homo sapiens (human)
DOID:2945	severe acute respiratory syndrome Aliases: SARS SARS-CoV infection	ABO ACE BST2 CALR CD14 CD209 FCER2 IL18R1 IL1R1 MASP2 MBL2 PI4KB SULT1E1 TLR2 TNF	10747 1636 2208 28 30835 3554 4153 5298 6783 684 7097 7124 811 8809 929	Homo sapiens (human)
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	G6pd2 G6pdx	14380 14381	Mus musculus (house mouse)
DOID:0112022	non-syndromic X-linked intellectual disability 21 Aliases: MRX21 MRX34 X-linked mental retardation 21 X-linked mental retardation 21/34 X-linked mental retardation 34	il1rapl1a il1rapl1b	557801 568868	Danio rerio (zebrafish)
DOID:11661	blue color blindness Aliases: Tritan defect Tritanopia	ACO2 CA4 CACNA2D4 ELOVL4 G6PD HS6ST1 MBD4 NYX PCYT1A SDHC STS	2539 412 50 5130 60506 6391 6785 762 8930 93589 9394	Homo sapiens (human)

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