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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 **2351 - 2375** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
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)	DisGeNET Alliance of Genome Resources
DOID:11258	cat-scratch disease Aliases: Debre's Syndrome Debre-Mollaret Syndrome Foshay-Mollaret Cat Scratch Fever benign lymphoreticulosis cat scratch fever	CALR PTGS2 SMUG1	23583 5743 811	Homo sapiens (human)	DisGeNET
DOID:12514	retinal perforation Aliases: Retinal break Retinal dialysis Retinal tear	GALNS RPE	2588 6120	Homo sapiens (human)	DisGeNET
DOID:9279	hyperhomocysteinemia	ACE ADH5 ALOX5 ATP1A2 CAT CYP1A1 CYP2J2 FOLR1 FOLR2 G6PD GPX1 GPX7 HSD11B1 ICAM1 MBL2 OLR1 PC PIK3CA PIK3CB PIK3CD PIK3CG PKM PTGS2 SHMT1 SLC33A1 SMPD1 VCAM1	128 1543 1573 1636 2348 2350 240 2539 2876 2882 3290 3383 4153 477 4973 5091 5290 5291 5293 5294 5315 5743 6470 6609 7412 847 9197	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0080198	infantile histiocytoid cardiomyopathy	IL1RL1	9173	Homo sapiens (human)	DisGeNET
DOID:10780	primary polycythemia Aliases: Familiar Polycythemia familial erythrocytosis	ACE CD177 FCER2 PKLR SLC17A5	1636 2208 26503 5313 57126	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0060639	permanent neonatal diabetes mellitus Aliases: PDMI PNDM permanent diabetes mellitus of infancy	GCK INS KCNJ11 SLC2A2	2645 3630 3767 6514	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:14069	cerebral malaria Aliases: Malarial encephalitis	ACE ALOX5 CAT CHI3L1 ENOSF1 FH ICAM1 IL1R1 ISYNA1 LGALS2 MBL2 MPPE1 PNP PRKAA2 PTGS2 SELE	1116 1636 2271 240 3383 3554 3957 4153 4860 51477 55556 5563 5743 6401 65258 847	Homo sapiens (human)	DisGeNET
DOID:216	dental caries Aliases: Dental caries extending into pulp Dental caries of smooth surface Dental caries pit and fissure	ACE AGA ALOX15 ALPL ATP6V0A2 ATP6V1A CALR CD14 COG6 COMT DAG1 FCN2 GALK2 GALNS GLB1 GLUL IDUA ITPKB LYZL2 MBL2 MTM1 MTMR3 NDUFAB1 OCRL PIGA PLA2G6 PSAP PTEN SGMS2 SLC2A2 SLC2A4 SRGN TMTC3	119180 1312 160418 1605 1636 166929 175 2220 23545 246 249 2585 2588 2720 2752 3425 3707 4153 4534 4706 4952 523 5277 5552 5660 5728 57511 6514 6517 811 8398 8897 929	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0110573	autosomal dominant nonsyndromic deafness 4A Aliases: DFNA4A autosomal dominant deafness 4A	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)	DisGeNET
DOID:4411	hepatitis E	BST2 CYP1A1 EXT1 HPGDS HSPG2 PSAP	1543 2131 27306 3339 5660 684	Homo sapiens (human)	DisGeNET
DOID:4160	differentiating neuroblastoma	CHAT	1103	Homo sapiens (human)	DisGeNET
DOID:0110770	hereditary spastic paraplegia 17 Aliases: SPG17 Silver spastic paraplegia syndrome Silver syndrome autosomal dominant spastic paraplegia 17 autosomal dominant spastic paraplegia type 17 dHMN5B distal hereditary motor neuropathy type 5B spastic paraplegia with amyotrophy of hands and feet spastic paraplegia-amyotrophy of hands and feet	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)	DisGeNET
DOID:0111275	speech-language disorder-1 Aliases: CAS articulatory apraxia childhood apraxia of speech developmental apraxia of speech developmental verbal dyspraxia speech and language disorder with orofacial dyspraxia speech-language disorder type 1	ACE ALDH2 B3GAT1 CHI3L1 FASN FCGR3B GALT LGALS1	1116 1636 217 2194 2215 2592 27087 3956	Homo sapiens (human)	DisGeNET
DOID:12559	idiopathic juvenile osteoporosis Aliases: Idiopathic osteoporosis juvenile osteoporosis	CYP19A1 LRP5	1588 4041	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:1245	vulva cancer Aliases: Ca vulva Vulvar tumor malignant Vulvar tumor malignant neoplasm of vulva malignant tumor of vulva neoplasm of vulva vulval cancer vulval neoplasm vulvar neoplasm	ABO AKT1 PTEN PTGS2 SMUG1	207 23583 28 5728 5743	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:12556	acute kidney tubular necrosis Aliases: ATN - acute tubular necrosis acute renal Failure with tubular necrosis acute renal failure with lesion of tubular necrosis acute tubular necrosis acute tubule necrosis	ARSA ARSD CHI3L1 MLYCD PTGS2	1116 23417 410 414 5743	Homo sapiens (human)	DisGeNET
DOID:0050453	lissencephaly	ALPP ATP6V0A2 ATP6V1A ATRNL1 B3GALNT2 B4GAT1 CD33 CD38 COMT CRPPA CYP2B6 DAG1 DHCR24 DLD DLST FCN2 FIG4 FKRP FKTN HSPG2 LARGE1 NSDHL OCRL PAFAH1B1 PIGA PIGN PIGP PIGQ PLCB1 PLCE1 PLCG1 POMGNT1 POMGNT2 POMK POMT1 POMT2 PTEN RXYLT1 SDC2 SLC17A5 STS TMTC3	10329 10585 11041 1312 148789 1555 160418 1605 1718 1738 1743 2218 2220 23236 23545 23556 250 26033 26503 29954 3339 412 4952 5048 50814 51196 51227 523 5277 5335 55624 5728 6383 729920 79147 84197 84892 9091 9215 945 952 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:4012	papillary transitional carcinoma Aliases: Papillary transitional cell carcinoma	AKR1C3 PKM PTEN	5315 5728 8644	Homo sapiens (human)	DisGeNET DisGeNET
DOID:8923	skin melanoma Aliases: cutaneous melanoma malignant ear melanoma malignant lip melanoma malignant lower limb melanoma malignant melanoma of ear and/or external auricular canal malignant melanoma of skin of lower limb malignant melanoma of skin of trunk except scrotum malignant melanoma of skin of upper limb malignant neck melanoma malignant scalp melanoma malignant trunk melanoma malignant upper limb melanoma	ACE ACER3 ACHE ACO1 ACSL3 AKR1B10 ALDH1A3 ALDH3A1 ALDH7A1 ALOX12 ALOX5 ALPI ALPP AMACR ANXA5 ANXA7 ANXA9 APRT ARSB ART3 ASAH1 B3GAT1 B4GALNT1 BST2 CALR CANX CAT CD14 CD1D CD22 CD248 CD38 CD44 CD74 CDH13 CEACAM5 CEACAM7 CERS2 CERS6 CH25H CHI3L1 CLEC10A CLEC14A CLEC1B CMAS CPT1A CPT1C CRYBG1 CSGALNACT1 CSPG4 CYP19A1 CYP1B1 CYP21A2 CYP24A1 CYP27B1 CYP2B6 CYP2E1 CYP2R1 DBT DERA DGKA DGKI DHCR24 EBP ECHDC1 EDEM1 EFNA1 ELOVL2 ENO2 ENPP1 FASN FCGR3B FDFT1 FDPS FOLR2 FUT1 FUT2 FUT4 FUT8 G6PD GALNT14 GALNT3 GAPDH GAPDHS GAS1 GBE1 GCNT2 GCNT3 GFRA1 GGT1 GLB1 GLO1 GLT8D1 GNS GOLPH3 GPAM GPAT2 GPC3 GPC6 GPLD1 GPNMB GPX1 GPX3 HADHB HAS2 HAS3 HK1 HMGCL HPGDS HPRT1 HPSE HS2ST1 HS3ST5 HSD11B1 HSD11B2 HSD17B12 HSPG2 HYAL2 ICAM1 IDH1 IDH2 IDUA IGF2R IL18R1 IL1RAPL1 INPP4B INPP5D INPP5E INPP5K ISYNA1 KL KLRB1 KLRC1 KLRK1 L1CAM LDHA LGALS1 LGALS3 LGALS9 LIPA LTA4H LYPD5 LYPLA1 LYPLA2 MAG MCAT MDH2 MELTF MGAT5 MGLL MICA MMP25 MOGS MPG MPPE1 MRC1 MTAP MUTYH NAMPT NCAM1 NEU1 NGLY1 NT5E OGG1 OS9 PARP1 PC PCK2 PCYT1A PDHB PDIA3 PFKFB2 PFKFB3 PFKFB4 PGK1 PIGU PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PKD1 PKM PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLAUR PLCB2 PLCB4 PLD1 PNP PNPLA2 PPP1R3B PRKAA2 PRNP PSMD10 PTEN PTGDS PTGES PTGS1 PTGS2 PYGM RECK RPE RTN4R SCD5 SCD SDC1 SDC2 SDC4 SDHA SDHB SDHC SDHD SELE SELL SEMA7A SGMS1 SIGLEC1 SIGLEC7 SIGLEC9 SIRT2 SIRT6 SLC17A5 SLC2A2 SLC2A3 SLC33A1 SMPD1 SMUG1 SOAT1 SPAM1 ST3GAL4 ST6GALNAC2 ST8SIA1 STS SULF1 TKTL1 TMED5 TNFRSF10C TPI1 UGT8 VCAM1 VCAN VTCN1	100507436 10082 1012 10135 10434 10457 10462 1048 10610 10682 10855 1087 10956 11141 1116 11313 11343 120227 126129 128869 1374 142 1462 1464 150763 1545 1555 1571 1588 1589 1591 1594 1606 161198 1629 1636 1718 1942 202 2026 218 2181 2194 220 2215 2222 2224 222537 22914 22933 23213 2350 23583 23600 239 240 248 250 2523 2524 2526 2530 253782 2539 2583 2591 259230 2597 2619 2632 26330 26503 2651 2674 2678 27036 27087 27180 2719 2720 27306 27349 2739 2799 2822 284348 2876 2878 2923 29956 3032 3037 3038 308 3098 310 3155 3251 3290 3291 3339 3383 3417 3418 3425 3482 353 3635 3820 3821 3897 3939 3956 3958 3965 3988 4048 4099 411 412 419 4191 4241 4249 427 43 4350 4360 4507 4595 4684 4758 48 4860 4907 4968 501 5091 50999 5106 51071 51144 51266 5130 51477 51548 5162 5167 51763 5208 5209 5210 5230 5289 5290 5291 5293 5294 5305 5310 5315 5319 5320 5321 5329 5330 5332 5337 54898 55331 5563 55768 55790 55830 55862 55907 5621 56623 57016 57104 57124 5716 5728 5730 5742 5743 57678 5837 6120 6319 6382 6383 6385 6389 6390 6391 6392 6401 6402 64083 64386 6484 6489 65078 6514 6515 65258 6609 6614 6646 6677 684 7167 7368 7412 7841 79623 79660 79679 79966 811 821 8277 8398 8416 8434 847 8482 8692 8794 8809 8821 9023 912 9162 9197 9245 929 933 9365 952 9536 960 9653 9695 972	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
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)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060475	myoclonic-atonic epilepsy Aliases: EEOC childhood onset epileptic encephalopathy	SLC25A10	1468	Homo sapiens (human)	Alliance of Genome Resources
DOID:115	cardiac tamponade Aliases: Rose's tamponade pericardial tamponade	PCYT1A SMUG1 SOAT1	23583 5130 6646	Homo sapiens (human)	DisGeNET DisGeNET
DOID:11338	tetanus Aliases: Infection due to Clostridium tetani clostridial tetanus	ABO	28	Homo sapiens (human)	DisGeNET
DOID:0111005	cone-rod dystrophy 2 Aliases: CORD2 CRD2 RCRD2 cone-rod retinal dystrophy 2 retinal cone-rod dystrophy 2	ALOX12 CACNA2D4 CD38 CNTN3 CNTN6 CYP19A1 ELOVL4 GAL3ST1 H6PD HSD11B1 LGALS1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN RGMA SIGLEC7 SLC35A1 SOAT1	10559 1588 239 27036 27255 3290 3956 5067 5290 5291 5293 5294 56963 5728 6646 6785 93589 9514 952 9563	Homo sapiens (human)	DisGeNET

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