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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 **6526 - 6550** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:305	carcinoma Aliases: epithelial cancer epithelioma malignant Epithelioma	ABO ACACA ACACB ACE ACSL1 ACSL5 ACSM1 ADH1B ADH1C ADH4 ADH5 AGXT AKR1B10 AKR1B1 AKR1C3 ALDH2 ALDH3A1 ALDH5A1 ALDH7A1 ALDOA ALOX15 ALOX15B ALOX5 ALPI ALPP AMACR ANXA4 ANXA5 APRT ARSA ASAH1 ATP6AP2 B3GAT1 B4GALNT2 BAAT C1GALT1 CACNA2D3 CALR CAT CBR1 CD109 CD14 CD1D CD248 CD33 CD38 CD44 CD55 CD74 CDH13 CDS1 CEACAM5 CEACAM6 CEACAM7 CERS2 CHGA CHPT1 COLEC10 CPT1A CPT2 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP1B1 CYP24A1 CYP27B1 CYP2E1 CYP3A5 CYP3A7 CYP4F3 DAG1 DBT DCN DCXR DHCR24 DHDH ECI1 EFNA1 ENO1 ENO2 ENPP1 ENPP3 FASN FBP1 FCGR3B FH FOLR1 FUT1 FUT3 FUT4 FUT6 G6PC1 GALNT3 GALNT6 GAPDH GCNT1 GGT1 GLB1 GLO1 GLUL GOLPH3 GPC3 GPLD1 GPX2 GPX3 GUSB HAGH HAS1 HAS2 HAS3 HK2 HMGCS2 HMMR HPGDS HPSE HSD17B12 HSD17B7 HSD3B1 HSPG2 HYAL1 HYAL2 HYAL3 ICAM1 IDH1 IDH2 INPP4B ITLN1 KLRK1 L1CAM LDHA LDHB LGALS1 LGALS3 LGALS4 LGALS8 LGALS9 LMAN1 LPCAT1 LPIN1 LPL LY6K LY75 LYPD5 LYPLA1 MAN2C1 MBD4 MCAT MDH2 MELTF MGAT5 MICA MINPP1 MMP25 MPG MRC1 MSLN MTAP MUTYH NAMPT NCAM1 NEIL1 NEU1 NEU3 NT5E NTHL1 OGG1 OPCML PARP1 PDHA1 PDIA3 PFKM PGAM1 PGK1 PGP PIGU PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G1B PLA2G2A PLA2G6 PLAUR PLCD1 PLCE1 PLCG1 PLD1 PLD2 PLPP2 PNP POFUT1 PPP1R3A PRKAA2 PRNP PRPS1 PSMD10 PTEN PTGDS PTGES3 PTGES PTGS1 PTGS2 PYGM QTRT1 RECK SCD SDC1 SELE SEMA7A SFTPC SHMT1 SIGLEC12 SIGLEC9 SIRT2 SIRT6 SLC2A2 SLC35A2 SMC3 SMUG1 SPAM1 SPHK1 SPHK2 SRGN ST3GAL4 ST3GAL6 ST6GAL1 ST8SIA4 STS SULF1 SULF2 SULT1E1 TKT TKTL1 TM7SF2 TNKS TYMP UGCG UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B7 UMPS VCAN VTCN1	100507436 1012 10135 10159 10232 1040 10402 10434 1048 10584 10728 10825 10855 1087 1113 11226 116285 124872 125 126 127 128 128869 135228 1374 1376 142 1462 1543 1544 1545 1551 1571 1577 1586 1588 1591 1594 1604 1605 1629 1632 1634 1636 1718 189 1890 1942 2023 2026 217 218 2180 2194 2203 2215 226 2271 22914 22933 231 23175 23213 2348 23509 23583 23600 240 246 247 248 250 2523 2525 2526 2528 2538 2591 2597 2650 2678 27087 27180 2719 2720 27294 27306 27349 2739 2752 28 2822 283871 284348 2877 2878 2923 2990 29956 3029 3036 3037 3038 307 308 3099 31 3158 3161 32 3283 3339 3373 3383 3417 3418 353 3897 3939 3945 3956 3958 3960 3964 3965 3998 4023 4051 4065 410 412 4123 4191 4241 4249 427 4350 4360 4507 4595 4680 4684 4758 4860 4907 4913 4968 4978 501 51144 51181 51196 51478 51548 5160 5167 5169 51703 5213 5223 5230 5289 5290 5291 5293 5294 5315 5319 5320 5329 5333 5335 5337 5338 54575 54576 54577 54578 54579 54600 54657 54658 54659 54742 5506 5552 55600 5563 55799 55959 5621 5631 56848 56886 56913 56994 570 57016 57124 5716 5728 5730 5742 5743 5837 6319 6382 6401 64083 64386 6440 6470 6480 6484 6514 6677 6783 7086 7108 7355 7357 7364 7372 7903 7915 79661 79679 79888 811 81890 8277 8372 8398 8434 847 8482 8612 8644 8658 8692 873 8821 8877 8930 89858 912 9126 929 945 952 9536 9562 960 972	Homo sapiens (human)
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	Hk1	15275	Mus musculus (house mouse)
DOID:10780	primary polycythemia Aliases: Familiar Polycythemia familial erythrocytosis	ACE CD177 FCER2 PKLR SLC17A5	1636 2208 26503 5313 57126	Homo sapiens (human)
DOID:11088	asphyxia neonatorum Aliases: Asphyxia - birth Asphyxia, in liveborn infant Birth asphyxia postnatal asphyxia	ALDH7A1 ALG8 CAT ENO2 HSD11B2 MTMR14 PDIA3 PTGS2	2026 2923 3291 501 5743 64419 79053 847	Homo sapiens (human)
DOID:5517	stomach carcinoma Aliases: cancer of the stomach carcinoma of stomach gastric carcinoma	parp-1	266823	Caenorhabditis elegans
DOID:0110580	autosomal dominant nonsyndromic deafness 54 Aliases: DFNA54 autosomal dominant deafness 54	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)
DOID:10871	age related macular degeneration Aliases: Age Related Maculopathies Age Related Maculopathy Senile macular degeneration Senile macular retinal degeneration age-related macular degeneration	ACAT1 ACE ACO1 AKR1A1 ALDH3A2 ALDH5A1 ATP6AP2 B3GLCT CALR CAT CD55 CHI3L1 CHST6 CYP1A2 CYP21A2 CYP24A1 CYP27A1 CYP2C19 CYP2R1 CYP46A1 ELOVL4 FADS1 FADS2 FCGR3B FCN2 FMOD FUT6 G6PD GALNS GPX3 HPGDS HS3ST4 HSD11B1 HSPG2 ICAM1 LGALS1 LIPC LPL MAN2B1 MASP1 MBL2 MUTYH NCAM1 OGG1 PARP12 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G12A PLCG2 PNPLA2 PPARGC1A PPT1 PTEN RENBP RPE SCD5 SELE SELL SELP SMUG1 SUCLA2 UGT2B17 UNG XYLT1 XYLT2	10159 10327 10858 10891 1116 120227 142 145173 1544 1557 1589 1591 1593 1604 1636 2215 2220 224 2331 23583 2528 2539 2588 27306 2878 3290 3339 3383 38 3956 3990 3992 4023 4125 4153 4166 4595 4684 48 4968 5290 5291 5293 5294 5336 5538 5648 57104 5728 5973 6120 6401 6402 6403 64131 64132 64761 6785 7367 7374 7915 79966 811 81579 847 8803 9415 9951	Homo sapiens (human)
DOID:0050749	peripheral T-cell lymphoma	CD1D CD44 CLEC10A CYP3A4 IDH1 IDH2 LGALS1 MTAP NCAM1 PIK3CA PIK3CB PIK3CD PIK3CG PNP SMUG1 SOAT1 TM7SF2	10462 1576 23583 3417 3418 3956 4507 4684 4860 5290 5291 5293 5294 6646 7108 912 960	Homo sapiens (human)
DOID:0111459	classic galactosemia Aliases: GALT deficiency galactose-1-phosphate uridyltransferase deficiency galactosemia type 1	ZK1058.3	175506	Caenorhabditis elegans
DOID:5082	liver cirrhosis Aliases: Cirrhosis cirrhosis of liver	ABO ACAT1 ACE ACHE ADH1A ADH1B ADH1C ADH4 ADH5 ADIPOQ AGA AGL AKR1A1 AKR1B10 AKR1B1 ALDH1B1 ALDH2 ALDH7A1 ALDOB ALOX5 ALPI ALPP ANXA5 APRT ARSH ATRNL1 CALR CAT CBR1 CD14 CD1D CD248 CD38 CD44 CD74 CDH13 CEACAM5 CEACAM7 CERS6 CHI3L1 CHIT1 CHST3 CLEC7A CMAS CPT1A CPT2 CYP17A1 CYP19A1 CYP1A1 CYP1A2 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2E1 CYP2R1 CYP3A4 CYP3A7 CYP4A11 CYP4F3 DCN DDOST DGKE DHCR7 DHDDS DLAT ENO1 ENPP2 EXTL3 FADS1 FCGR3B FCN2 FDFT1 FMOD FUT1 GALT GBA1 GCDH GCK GCLC GGT1 GLB1 GLO1 GLT8D2 GLUL GNPAT GOLPH3 GPAA1 GPC3 GPD1 GPNMB GPX1 HACD1 HAS2 HEXB HK2 HMGCS2 HPGDS HPSE HSD11B2 HSPG2 ICAM1 IDH1 IGF2 IGF2R IL1R1 INPP5D INPP5E ISYNA1 KL LALBA LDHA LGALS1 LGALS3 LGALS8 LGALS9 LIPA MASP1 MBL2 MBOAT7 MICA MLYCD MPI MSLN MTAP NAAA NAGLU NAMPT NANS NCAM1 NCAN NDST1 NT5E OGA OGT PARP1 PC PDIA3 PEMT PHKG2 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLAUR PLB1 PMM2 PNPLA3 PNPLA6 PRKAA2 PSMD10 PTEN PTGDS PTGIS PTGS2 RBP4 RENBP RGN SCD SDC1 SDC2 SDC4 SFTPA1 SIGLEC1 SIRT2 SLC17A5 SLC27A5 SLC2A4 SLC33A1 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 ST6GAL1 ST8SIA4 STS SULF1 TALDO1 TBXAS1 TLR4 TM7SF2 TNF TYMP UGT1A1 UGT1A7 UMOD VCAM1	100507436 1012 10135 10232 10327 10400 10457 1048 10724 10855 1087 10908 10998 1116 1118 120227 124 125 126 127 128 1374 1376 142 1463 151056 1543 1544 1551 1555 1557 1571 1576 1579 1586 1588 1593 1594 1634 1636 1650 1717 1737 175 178 1890 2023 2137 217 219 2215 2220 2222 229 22933 231 23213 2331 23417 23583 240 248 250 2523 253782 2592 26033 2629 2639 2645 26503 2678 27163 2719 2720 2729 27306 2739 2752 28 2819 2876 2923 3037 3074 308 3099 3158 3291 3339 3340 3383 3417 347527 3481 3482 353 3554 3635 38 3906 3939 3956 3958 3964 3965 3988 3992 4051 412 4153 43 4351 4507 4669 4684 4907 501 5091 51477 5168 5261 5290 5291 5293 5294 5315 5319 5320 5321 5329 5373 54187 54577 54658 5563 55907 5648 56623 56848 57016 57124 5716 5728 5730 5740 5743 5950 5973 6319 6382 6383 6385 64083 64581 6480 6517 653509 6609 6614 6646 6888 6916 7099 7108 7124 7369 7412 7903 79143 79947 80339 811 83468 8398 8443 847 8473 8526 873 8733 8877 9104 912 9197 9200 929 9365 9370 9469 952 960 972	Homo sapiens (human)
DOID:11338	tetanus Aliases: Infection due to Clostridium tetani clostridial tetanus	ABO	28	Homo sapiens (human)
DOID:2280	hidradenitis suppurativa Aliases: Acne inversa, familial	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:9269	maple syrup urine disease Aliases: Ketoacidaemia branched chain ketoaciduria	BCKDHA BCKDHB CACNA2D2 CYB5R3 DBT DLD HADH LPL UMOD	1629 1727 1738 3033 4023 593 594 7369 9254	Homo sapiens (human)
DOID:0081312	T-cell non-Hodgkin lymphoma	Ier3 Tmem260 Trp53	15937 218989 22059	Mus musculus (house mouse)
DOID:13405	cardiac sarcoidosis	CALR SMUG1	23583 811	Homo sapiens (human)
DOID:0050570	congenital disorder of glycosylation type I	alg12 alg1 alg5 alg6 alg8 alg9 dpm1	100497477 448472 496884 496948 548388 548874 594994	Xenopus tropicalis (tropical clawed frog)
DOID:11119	Gilles de la Tourette syndrome Aliases: Guinon's disease Psychogenic tics Tourette syndrome motor-verbal tic disorder	ALG9 CHAT CNTN6 COMT ENO2 GPC5 HEXD HK1 HPGDS IL1R1 LCT LYPD6 OGA PARP1 PARP9 PKM	10724 1103 130574 1312 142 2026 2262 27255 27306 284004 3098 3554 3938 5315 79796 83666	Homo sapiens (human)
DOID:713	HCL-V Aliases: Hairy cell leukaemia variant Hairy cell leukemia variant	ACSBG1 ANXA5 B3GAT1 CD1D CD22 CD44 CYP19A1 ENPP1 HEXB NCAM1 NDUFAB1 PIK3CA PIK3CB PIK3CD PIK3CG SMUG1	1588 23205 23583 27087 3074 308 4684 4706 5167 5290 5291 5293 5294 912 933 960	Homo sapiens (human)
DOID:1727	retinal vein occlusion Aliases: Occlusion, of retinal vein	ACE CYP1B1 HPSE PNP VCAM1	10855 1545 1636 4860 7412	Homo sapiens (human)
DOID:12549	hepatitis A Aliases: Viral hepatitis, type A	Tnf	21926	Mus musculus (house mouse)
DOID:10247	pleurisy	ALOX5 ICAM1 MTAP PIK3CG PLA2G10 PLA2G2A PLA2G6 PTGS2 TNF TPI1	240 3383 4507 5294 5320 5743 7124 7167 8398 8399	Homo sapiens (human)
DOID:12271	aniridia Aliases: Aplasia of iris isolated aniridia	ADH7 ARSD CAT CYP1B1 DLST FH GPC3 LDHD MDH2 SDHA SDHB SDHC SDHD	131 1545 1743 197257 2271 2719 414 4191 6389 6390 6391 6392 847	Homo sapiens (human)
DOID:0070384	developmental and epileptic encephalopathy 98 Aliases: DEE98 early infantile epileptic encephalopathy 98	Atp1a2	24212	Rattus norvegicus (Norway rat)
DOID:0110746	type 1 diabetes mellitus 7 Aliases: IDDM7 Insulin-Dependent Diabetes Mellitus 7	ABO ACAN ACE ACOT7 ACSL1 ADH5 AGA AGPAT1 AKR1A1 AKR1B1 ALDH2 ALDH3A2 ALOX12 ALOX15B ALOX5 AMY2A ANXA5 APRT B3GAT1 B4GALNT1 B4GALT1 BAAT CAT CBR1 CD14 CD1D CD209 CD38 CD44 CD48 CD74 CDH13 CEACAM5 CEPT1 CHAT CHST3 CLEC16A CSGALNACT1 CYP21A2 CYP24A1 CYP27A1 CYP27B1 CYP2E1 CYP2R1 CYP7A1 DCN DDOST DGCR2 DHCR7 DLAT EFNA1 ENO2 ENPP1 FASN FCER2 FCGR3B FCN2 FKRP FUT2 G6PC1 G6PC2 G6PD GAD1 GAD2 GAL3ST1 GALNT3 GBA3 GCK GLA GLB1 GLO1 GLUL GPI GPX1 GPX3 GYS1 HK1 HK2 HMGCS2 HPGDS HPRT1 HPSE2 HPSE HSD11B1 HSD11B2 HSD17B4 HSPG2 ICAM1 IGF2R IL18R1 IL18RAP IL1R1 IL1RL1 INPP5D INPPL1 IPPK ISYNA1 KL KLRC3 KLRD1 LDHC LGALS1 LGALS3 LIPC LPL LY6G6D LYPD5 MASP2 MBL2 MGAT1 MGAT5 MICA MIOX NAAA NAMPT NCAM1 OGA PARP1 PDHX PFKFB3 PGM1 PGP PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2C PLA2G6 PLA2G7 PNPLA3 PRKAA2 PRKCSH PTEN PTGS2 REG1B RENBP SCD SDC2 SELE SELL SELP SIRT2 SIRT6 SLC2A12 SLC2A2 SLC2A3 SLC2A4 SLC2A8 SLC35A1 SLC35G1 SLC37A4 SLC5A1 SOAT1 ST3GAL4 SULT1E1 TKT TM7SF2 UGT1A1 UMOD VCAM1 VCAN VTCN1 XYLT1 XYLT2	100507436 1012 10135 10327 10390 1048 10554 10559 10724 10747 10855 1103 11332 120227 128 142 1462 154091 1571 1581 1589 1591 1593 159371 1594 1634 1636 1650 1717 1737 175 176 1942 2026 217 2180 2194 2208 2215 2220 224 22933 231 23274 239 240 247 2524 2538 2539 2542 2571 2572 2583 2591 2645 2683 27087 27163 2717 2720 27306 2739 2752 279 28 2821 283871 284348 2876 2878 2997 29988 308 30835 3098 3099 3158 3251 3290 3291 3295 3339 3383 3482 353 3554 3635 3636 3823 3824 3948 3956 3958 3990 4023 4153 4245 4249 4684 51477 51548 5167 5209 5236 5290 5291 5293 5294 54658 55586 5563 55790 5589 570 5728 5743 57733 57818 58530 5968 5973 60495 6319 6383 6401 6402 6403 64131 64132 64768 6484 6514 6515 6517 6523 6646 6783 7086 7108 7369 7412 79147 7941 79679 79837 80339 8050 8398 847 873 8807 8809 912 9173 929 9365 9469 9514 952 960 962 972 9993	Homo sapiens (human)
DOID:0080349	developmental and epileptic encephalopathy 39 Aliases: AGC1 deficiency early infantile epileptic encephalopathy 39 epileptic encephalopathy with global cerebral demyelination	ACAN SLC25A12	176 8604	Homo sapiens (human)

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