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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 **4076 - 4100** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲
DOID:1883	hepatitis C Aliases: NANBH Viral hepatitis C chronic hepatitis C hepatitis C infection hepatitis nonA nonB	ABO ACACA ACAT1 ACAT2 ACE ACSL3 ADH1A ADH1B ADH4 AGA AGL AKR1A1 AKR1B10 AKR1B1 ALDH2 ALDH7A1 ALG10 ALPP APRT ARF4 ATRNL1 B3GAT1 BST2 CAT CD14 CD1D CD209 CD33 CD38 CD44 CD55 CEL CH25H CHI3L1 CHIT1 CHPT1 COMT CPT1A CPT2 CRLS1 CYP17A1 CYP1A1 CYP1A2 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2C19 CYP2C9 CYP2E1 CYP2R1 CYP3A4 CYP3A5 CYP4F3 DDOST DGAT1 DGAT2 DHCR24 DHCR7 EBP EDEM1 EDEM3 ENPP1 ENPP2 EXT1 FASN FBP1 FCGR3B FCN2 FUT1 FUT8 G6PC1 GALNT8 GAPDH GFRA1 GGT1 GLT8D2 GLTP GOLPH3 GP2 GPC3 GPX1 GPX2 GUSB HACD1 HADHA HJV HK2 HMGCS1 HMGCS2 HPGDS HPSE2 HPSE HSPG2 ICAM1 IL1R1 IL1RAPL2 IL1RL2 INPPL1 ISYNA1 KLRB1 KLRC1 KLRD1 KLRK1 LGALS1 LGALS3 LGALS4 LGALS9 LIPA LPCAT1 LPL LY75 MASP1 MASP2 MBL2 MBOAT7 MICA MPG MRC1 NAAA NCAM1 NCAN NEIL1 NEIL2 OGG1 OGT PCK2 PCYT1A PDIA3 PI4KA PI4KB PIK3C2B PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G1B PLA2G4C PLB1 PNPLA3 PRNP PSMD10 PTEN PTGES3 PTGS2 QPRT RECK RENBP SCD SDC1 SDC2 SDC3 SDC4 SDHC SIGLEC1 SLC17A5 SLC2A2 SLC35A2 SOAT1 SRD5A2 STS TM7SF2 TMED5 UGGT1 UGT1A1 UGT1A7 ULBP1 VCAN	100507436 10327 1056 10682 10728 10747 10855 1116 1118 120227 124 125 127 1312 1374 1376 1462 1463 148738 151056 1543 1544 1555 1557 1559 1571 1576 1577 1586 1591 1593 1594 1604 1636 1650 1717 1718 175 178 2131 217 2181 2194 2203 2215 2220 22914 231 23475 250 2523 252969 2530 2538 2597 26033 26280 26290 26503 2674 2678 27087 27163 2719 27306 28 2813 2876 2877 2923 2990 3030 30835 3099 31 3157 3158 3339 3383 353 3554 3636 378 38 3820 3821 3824 39 3956 3958 3960 3965 3988 4023 4051 4065 412 4153 4350 4360 4684 4968 501 50999 5106 51228 5130 51477 5167 5168 5287 5289 5290 5291 5293 5294 5297 5298 5315 5319 54577 54658 54675 5621 5648 56886 56994 57016 5716 5728 5743 5973 60495 6319 6382 6383 6385 6391 64083 6514 6614 6646 6716 684 7108 7355 79143 79661 79888 80267 80329 80339 83468 8434 84649 847 8473 84920 8605 8694 8808 9023 912 9200 929 945 952 960 9672 9695	Homo sapiens (human)
DOID:1929	supravalvular aortic stenosis Aliases: Supra-valvular aortic stenosis	ARSD CACNA2D1	414 781	Homo sapiens (human)
DOID:7998	hyperthyroidism Aliases: overactive thyroid	ABO ACACA ACE ADIPOQ ALG1 ANXA5 APRT ATP6AP2 B3GNT2 BAAT BDH1 CALR CAT CD14 CMAS COMT CS CYP19A1 CYP1A1 CYP21A2 CYP27B1 CYP2C9 CYP2R1 CYP7A1 DEGS1 ENPP2 FCER2 FCGR3B FUT2 GAD1 GAD2 GLO1 GLUL GPX1 ICAM1 IL18R1 IL18RAP IL1RL1 KLRC1 LGALS9 LYZ MBL2 NAMPT NCAM1 NR1D1 NT5E OGG1 PARP1 PC PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G2A PLA2G6 PPARGC1A PPT1 PRKAA2 PTEN PTGDS SCD SELE SELL SIGLEC1 SLC2A3 SLC2A4 SMUG1 ST3GAL1 ST6GAL1 TM7SF2 UGDH UGT1A1 UGT2B17 VCAM1	10135 10159 10678 10891 120227 1312 142 1431 1543 1559 1581 1588 1589 1594 1636 2208 2215 23583 2524 2571 2572 2739 2752 28 2876 308 31 3383 353 3821 3965 4069 4153 4684 4907 4968 5091 5130 5168 5290 5291 5293 5294 5319 5320 54658 5538 5563 55907 56052 570 5728 5730 622 6319 6401 6402 6480 6482 6515 6517 6614 7108 7358 7367 7412 811 8398 847 8560 8807 8809 9173 929 9370 9572	Homo sapiens (human)
DOID:0081381	juvenile amyotrophic lateral sclerosis type 27	SPTLC1	10558	Homo sapiens (human)
DOID:0070140	autosomal recessive cutis laxa type IIC	ATP6AP1 ATP6V0A2 ATP6V1A B3GALT6 B3GAT3 B4GALT7 CAT CHST3 DCN DHCR7 ECHS1 ENOSF1 MAN1B1 PARP1 PIGL PLCG2 PMM2 PTDSS1 SLC2A10 SRD5A3	11253 11285 126792 142 1634 1717 1892 23545 26229 523 5336 537 5373 55556 79644 81031 847 9469 9487 9791	Homo sapiens (human)
DOID:9428	intracranial hypertension Aliases: Raised intracranial pressure	ENO2 GLB1 L1CAM PARP4 PIK3CA PTEN SDHB SDHC	143 2026 2720 3897 5290 5728 6390 6391	Homo sapiens (human)
DOID:10915	Wernicke-Korsakoff syndrome Aliases: Korsakoff Syndrome Korsakoff's psychosis Korsakoff's syndrome Korsakov psychosis Korsakov's psychosis	ACACA ADH1B AKR1A1 ALDH2 CAT COMT CYP19A1 DLST GAD1 GLUL PIK3CA PIK3CB PIK3CD PIK3CG PNPLA3 TKT	10327 125 1312 1588 1743 217 2571 2752 31 5290 5291 5293 5294 7086 80339 847	Homo sapiens (human)
DOID:0110720	neuronal ceroid lipofuscinosis 4 Aliases: CLN4B disease autosomal dominant neuronal ceroid lipofuscinosis 4B neuronal ceroid lipofuscinosis 4 Parry type neuronal ceroid lipofuscinosis 4B	ACLY ARSG CLN5 EPM2A GAD1 GAD2 LGALS1 PKD1 PPT1 PPT2 PSAP	1203 22901 2571 2572 3956 47 5310 5538 5660 7957 9374	Homo sapiens (human)
DOID:8504	impetigo	GALNS	2588	Homo sapiens (human)
DOID:0070186	Y-linked spermatogenic failure 1 Aliases: SPGFY1 Y-linked Sertoli cell-only syndrome type I Sertoli cell-only syndrome	ANXA5 CYP17A1 CYP2R1 EPHX2 HPGDS LCT LDHC PARP1 PGAM1 PRPS2 SRD5A2 SRGN STS TEX101	120227 142 1586 2053 27306 308 3938 3948 412 5223 5552 5634 6716 83639	Homo sapiens (human)
DOID:0040091	autoimmune pancreatitis	ALPI ALPP AMY2A ENO1 PKD1 SMUG1	2023 23583 248 250 279 5310	Homo sapiens (human)
DOID:11406	choroiditis	ACE ICAM1	1636 3383	Homo sapiens (human)
DOID:0050785	progressive relapsing multiple sclerosis Aliases: PRMS Progressive-relapsing MS	LGALS3 RGMA SOAT1	3958 56963 6646	Homo sapiens (human)
DOID:0080362	X-linked spondyloepiphyseal dysplasia tarda	ACAN CD38 CHST3 GLB1 HSPG2	176 2720 3339 9469 952	Homo sapiens (human)
DOID:10579	leukodystrophy	ABAT ACER3 ACOT12 ACOX1 ARSA ATRN DAG1 DEGS1 ECHS1 GALC GBE1 HSD17B4 MAG PC PDHA1 PLA2G1B PLA2G6 PLB1 PSAP SDHA SDHB SLC17A5 SORD TYMP	134526 151056 1605 18 1890 1892 2581 2632 26503 3295 4099 410 5091 51 5160 5319 55331 5660 6389 6390 6652 8398 8455 8560	Homo sapiens (human)
DOID:1074	kidney failure Aliases: renal failure	A4GALT ACE ACSL4 ACSS2 AGL AGPAT2 AGXT AKR1B1 ALOX12B ALOX5 ALPP APRT ARSA ATP6AP2 ATRNL1 CAT CHGA COG1 CPM CPT2 CTNS CTSA CYP11B2 CYP1A2 CYP24A1 CYP2C19 CYP2C9 CYP3A4 CYP3A5 CYP4F3 DCN DEGS1 DGKE DHDDS EBP ENPP1 FCGR3B G6PC1 GCNT2 GGT1 GLA GRHPR HAGH HPRT1 HPSE2 HPSE HSD11B2 HSPG2 ICAM1 IDH2 INPP5E KL KLB LCAT LDHA LGALS3 LYZ MASP1 MBL2 ME1 MMUT MSLN NAGLU NAMPT NCAN OCRL OGA OLR1 PARP1 PGAM2 PGK1 PIK3C3 PKD1 PKD2 PLA2G15 PLA2G7 PNPLA3 PNPLA6 PPARGC1A PRKAA2 PRPS1 PTGS1 PTGS2 PYGM RENBP RGN SDC1 SDC2 SELE SELL SELP SLC17A5 SLC2A2 SLC35G1 SLC37A4 SLC3A1 SLC5A1 SMC3 SMUG1 STS SULT2B1 TLR2 TLR4 TM7SF2 TMEM260 UGT2B17 UMOD VCAM1 VCAN XYLT1 XYLT2	10135 10159 10232 10555 10682 10724 10855 10891 10908 1113 1368 1376 142 1462 1463 1497 152831 1544 1557 1559 1576 1577 1585 1591 159371 1634 1636 178 189 2182 2215 231 23583 23659 240 242 250 2538 2542 26033 26503 2651 2678 2717 3029 3251 3291 3339 3383 3418 353 3931 3939 3958 4051 4069 410 412 4153 4199 4594 4669 4952 4973 5167 5224 5230 5289 5310 5311 53947 5476 54916 5563 55902 5631 5648 56623 5742 5743 5837 5973 60495 6382 6383 6401 6402 6403 64131 64132 6514 6519 6523 6820 7097 7099 7108 7367 7369 7412 7941 79947 80339 847 8526 8560 9104 9126 9365 9380 9382	Homo sapiens (human)
DOID:1555	urticaria	ACE AGXT ALDH3A2 ALOX5 ARSA BST2 CAT CD38 DGKG ELOVL4 FCGR3B GPX1 HPGDS ICAM1 LTC4S PIGT PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLCG1 PLCG2 PTGS2 SDHB SDHC SELE VCAM1	1608 1636 189 2215 224 240 27306 2876 3383 4056 410 51604 5290 5291 5293 5294 5321 5335 5336 5743 6390 6391 6401 6785 684 7412 847 952	Homo sapiens (human)
DOID:5870	eosinophilic pneumonia Aliases: Pneumonia, eosinophilic	ALPL CEL CHI3L1 HPGDS IL1R1 IL1RL1 ISYNA1 PARP9 PTGDS SIGLEC8 SIRT2 SLC27A5	1056 10998 1116 22933 249 27181 27306 3554 51477 5730 83666 9173	Homo sapiens (human)
DOID:0110498	autosomal recessive nonsyndromic deafness 4 Aliases: DFNB4 autosomal recessive deafness 4 with enlarged vestibular aqueduct	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP RENBP SMUG1 TECTA	135228 146183 220074 22856 23583 25839 340990 410 50 51 5660 5973 7007	Homo sapiens (human)
DOID:0060432	chromosome 17p13.3 duplication syndrome Aliases: 17p13.3 duplication syndrome 17p13.3 microduplication syndrome chromosome 17p13.3 centromeric duplication syndrome trisomy 17p13.3	PAFAH1B1	5048	Homo sapiens (human)
DOID:9120	amyloidosis Aliases: amyloid disease	ACAN ACAT1 ACE ACHE ADIPOQ AGPS AKR1C4 ALOX12 ALOX15 ALOX5 ANXA5 APRT ARSA CAT CD109 CD14 CD33 CD38 CD55 CD74 CHAT CHI3L1 CHIT1 CHST6 CLEC7A CYP46A1 DCN DEGS1 DGCR2 DPEP1 EHHADH FCN2 G6PD GALNS GAPDH GOT1 GPNMB GPX1 HSD11B1 HSPG2 LYZ MAG MBL2 MICA NAGLU NCAM1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLA2G7 PLD3 PRNP PTGS1 PTGS2 SCD SDC1 SFTPA1 SLC2A12 SMUG1 SOAT1 STS SUCLA2 TNF VCAM1	100507436 10457 10858 1103 1109 1116 1118 135228 142 154091 1604 1634 1636 176 1800 1962 2220 23583 23646 239 240 246 2539 2588 2597 2805 2876 308 3290 3339 353 38 4069 4099 410 412 4153 4166 43 4669 4684 5290 5291 5293 5294 5321 5621 5742 5743 6319 6382 64581 653509 6646 7124 7412 7941 847 8540 8560 8803 929 9370 945 952 972 9993	Homo sapiens (human)
DOID:9111	cutaneous leishmaniasis Aliases: Asian Desert Cutaneous Leishmaniasis Leproid leishmaniasis diffuse cutaneous leishmaniasis	CAT CLEC7A DPAGT1 FCN2 FDPS FH G6PD PGD PNP SLC5A1 TLR2 TLR4 TNF	1798 2220 2224 2271 2539 4860 5226 64581 6523 7097 7099 7124 847	Homo sapiens (human)
DOID:1588	thrombocytopenia	ABO ACHE ADH1B ALG8 ASGR1 BAAT C1GALT1 CAT CD209 CD44 CD72 CEACAM5 CLEC1B COG1 COG4 COG6 COMT CYP2C8 CYP3A4 DGKE EFNA5 ELOVL4 EOGT FCGR3B G6PC3 GALE GBA1 GGT1 GNE HPSE HSPG2 KDSR MBD4 MBL2 MMUT MPI MRC1 MYORG NAAA NCAM1 OCRL PCCA PCCB PIK3C2A PIK3CA PIK3CB PIK3CD PMM2 PNLIP PSAP PTEN PTGS1 PTGS2 SC5D SELP SLC17A5 SLC35A1 SOAT1 SPHK2 STT3B TALDO1 TBXAS1 TNF UGT1A1 XYLT2	10020 1048 10559 10855 125 1312 1558 1576 1946 201595 2215 2531 2582 25839 2629 26503 2678 27163 28 285203 30835 3339 4153 43 432 4351 4360 4594 4684 4952 5095 5096 51266 5286 5290 5291 5293 5373 5406 54658 5660 56848 56913 570 5728 5742 5743 57462 57511 6309 6403 64132 6646 6785 6888 6916 7124 79053 847 8526 8930 92579 9382 960 971	Homo sapiens (human)
DOID:13709	premature ejaculation	ACE ACHE ACSS2 ALDH7A1 CDH13 COMT CYP19A1 ENO2 HEXB HJV HMGCS2 HS6ST1 LPL PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PNPLA2 SDC1 SOAT1	1012 1312 148738 1588 1636 2026 23659 3074 3158 4023 43 501 5130 5290 5291 5293 5294 55902 57104 6382 6646 9394	Homo sapiens (human)
DOID:0080555	congenital disorder of glycosylation Ic Aliases: congenital disorder of glycosylation 1c	ALG6	29929	Homo sapiens (human)

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