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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 **5676 - 5700** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:0060249	scoliosis	ACADS ACAN AGA AGPAT2 AGRN ALDH3A2 ALG11 ALG14 ALG1 ALG2 ASAH1 ATP6AP2 ATP6V0A2 B3GALT6 B3GAT3 B3GLCT B4GALNT1 B4GALT7 CD38 CHAT CHI3L1 CHST11 CHST14 CHST3 COG1 COG8 COLEC10 COLEC11 COMT CRPPA CYP7B1 DEGS1 DHCR7 DPAGT1 DPM2 EBP ENPP1 EXT1 EXT2 EXTL3 FKRP FKTN FUCA1 FUT8 GAD1 GALNS GAS1 GBA2 GFPT1 GLB1 GMPPB GNE GNPAT GNPTAB GNPTG GPC3 GPC5 GUSB HACD1 HGSNAT HSD17B4 HSPG2 IDH1 IDH2 IDUA INPP5E INPP5K INPPL1 LARGE1 LFNG MASP1 MTM1 MTMR2 NEU1 NGLY1 NSDHL OCRL PAPSS2 PCYT1A PGAP2 PGAP3 PGM3 PIGL PIGO PIGT PIGU PIGV PIGW PIGY PIK3C2A PIK3CA PLOD3 PMM2 POMK POMT1 POMT2 PRPS1 PTDSS1 PTEN SDHB SDHC SDHD SGMS2 SLC26A2 SLC2A10 SLC35A2 SLC35A3 SYNJ1 TGDS TMEM165 XYLT1	10020 10159 10555 10584 10585 10682 1103 1116 11285 113189 126792 128869 1312 138050 145173 166929 1717 175 176 1798 1836 199857 2131 2132 2137 2218 224 2262 23443 23483 23545 2517 2530 2571 2583 2588 2619 26229 2673 2719 2720 27315 284098 2990 29925 29954 3295 3339 3417 3418 3425 35 3636 375790 3955 427 440138 4534 4758 4952 50515 50814 5130 51604 5167 51763 5238 5286 5290 5373 55650 55768 55858 56052 5631 5648 56623 5728 57704 6390 6391 6392 64131 729920 7355 78989 79147 79158 81031 84197 84342 8443 84572 84720 84992 85365 8560 8818 8867 8898 8985 9060 9200 9215 93210 9382 9420 9469 9487 952 9791	Homo sapiens (human)	DisGeNET DisGeNET
DOID:9335	scotoma Aliases: Blind spot area scotoma Enlarged angioscotoma Enlarged blind spot Enlarged paracaecal scotoma Generalized visual field contraction or constriction Scotoma of blind spot area Sector or arcuate visual field defects	ARSG	22901	Homo sapiens (human)	DisGeNET
DOID:5434	scrapie	PRNP	5621	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:4423	sea-blue histiocytosis Aliases: Sea-blue histiocyte syndrome	GLB1 SMPD1	2720 6609	Homo sapiens (human)	DisGeNET
DOID:5759	sebaceous gland neoplasm Aliases: Sebaceous neoplasm	MRC1	4360	Homo sapiens (human)	DisGeNET
DOID:8941	seborrheic infantile dermatitis Aliases: Complement 5 dysfunction Generalized seborrheic dermatitis of infants Infantile seborrheic dermatitis Infantile seborrhoeic dermatitis Pityriasis capitis Seborrhea sicca Seborrhoea capitis Seborrhoeic dermatitis of scalp Seborrhoeic eczema of scalp cradle cap seborrhea capitis	COMT CYP51A1 PIK3CA	1312 1595 5290	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:11832	visual epilepsy Aliases: epilepsy, visual	ABAT ABO ACACA ACADM ACADS ACADSB ACAT1 ACE ACHE ACO2 ACOT7 ACOX1 ACSL4 ACSM3 ADPRS AGA AGPS AGRN ALDH3A2 ALDH5A1 ALDH7A1 ALDOB ALG11 ALG13 ALG1 ALG2 ALG3 ALG6 ALG9 ALPL AMACR AMT APEX1 ARSA ARSD ATP6AP2 ATP6V0A2 ATP6V1A B3GALNT2 B3GLCT BAD BCKDHA BCKDHB CAT CD38 CD44 CERS1 CHAT CLEC7A CLN5 CNTN2 CNTN4 COG2 COG5 COG6 COG8 COLGALT1 COMT CPT1A CPT2 CRPPA CTSA CYB5R3 CYP11A1 CYP1A1 CYP1A2 CYP27A1 CYP2C19 CYP2E1 CYP3A4 CYP4F3 DAG1 DBT DDOST DEGS1 DGCR2 DGKD DGKE DHCR24 DHDDS DLD DPAGT1 EBP ECHS1 ELOVL4 ENO2 EOGT EXT1 EXT2 FBP1 FCSK FDFT1 FH FKRP FKTN FUCA1 FUT8 G6PC1 G6PD GAD1 GAD2 GALC GAS1 GCDH GCK GCSH GLA GLB1 GLDC GLO1 GLUL GLYCTK GM2A GMPPA GMPPB GNE GNS GPAA1 GPC1 GPC3 GYS1 GYS2 HADHA HADHB HEXA HEXB HGSNAT HIBCH HMGCL HMGCS2 HPGDS HPRT1 HS6ST1 HSD17B4 ICAM1 IDH1 IDH2 IDS IL1RAPL1 IL6ST IMPA1 INPP5E ISYNA1 KCNJ11 L2HGDH LARGE1 LGALS3 LMAN2L LSS MAN1B1 MANBA MBL2 MBOAT7 MCAT MDH2 ME1 MGAT1 MGAT2 MGLL MICA MLYCD MMUT MOGS MPI MRC1 MTM1 MYORG NAGA NAGLU NDST1 NEU1 NGLY1 NPL NPY1R NRN1L NSDHL NT5E NTNG1 OCRL OGA PAFAH1B1 PC PCCA PCCB PCK1 PCYT1A PDHA1 PDHX PDIA3 PGAP1 PGAP2 PGAP3 PGK1 PGM3 PIGA PIGB PIGC PIGG PIGH PIGL PIGM PIGN PIGO PIGP PIGQ PIGS PIGT PIGU PIGV PIGW PIGY PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PLA2G10 PLA2G1B PLA2G2A PLA2G4A PLA2G6 PLAUR PLCB1 PLCG1 PLD1 PLD2 PMM2 PNPLA6 POMGNT1 POMGNT2 POMK POMT1 POMT2 PPT1 PRNP PRPS1 PSAP PSMD10 PTEN PTGES PTGS1 PTGS2 REG3G RFT1 RGMA RPIA RXYLT1 SACM1L SC5D SDHA SDHC SDHD SEMA7A SGPL1 SGSH SLC17A5 SLC2A3 SLC33A1 SLC35A1 SLC35A2 SLC35A3 SLC39A8 SLC3A1 SMC3 SMUG1 SRD5A3 ST3GAL3 ST3GAL5 STS STT3A STT3B SUCLA2 SUCLG1 SUMF1 SYNJ1 TECR TGDS TMED9 TMTC3 TNF TPI1 TUSC3 UGCG UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B7 UGT8	10020 100507436 10159 10195 10329 10466 10559 10585 10682 10715 10724 10908 1103 11141 11253 11332 11343 1203 123904 128869 130120 1312 132158 1374 1376 138050 145173 148789 152330 1543 1544 1557 1571 1576 1583 1593 160418 1605 1629 1636 1650 1718 1727 1738 175 1798 18 1892 197258 201595 2026 2131 2132 2182 2203 2218 2222 224 2271 22796 22854 229 22908 22934 23236 23417 23443 23483 23545 23556 23583 23600 249 2517 2530 2538 2539 2571 2572 2581 2619 26275 2639 2645 26503 2653 2717 2719 2720 27306 2731 27315 27349 2739 275 2752 2760 2799 28 2817 284098 285203 285362 2923 29925 29926 29929 29954 2997 2998 3030 3032 3073 3074 31 3155 3158 3251 328 3295 3340 3383 34 3417 3418 3423 35 3572 36 3612 3703 375790 3767 38 3958 4047 4051 410 412 4126 414 4153 4191 4199 4245 4247 43 4351 4360 440138 4534 4594 4668 4669 4758 4886 4907 4952 50 501 5048 50814 5091 5095 5096 51 5105 51227 5130 51477 5160 51604 523 5230 5238 5277 5279 5283 5290 5291 5293 5294 5310 5319 5320 5321 5329 5335 5337 5338 5373 54575 54576 54577 54578 54579 54600 54657 54658 54659 54732 5476 54872 54936 5538 55624 55650 55768 56052 5621 5631 5660 56623 56886 56963 5716 572 5728 5742 5743 57462 57511 593 594 6296 6309 6389 6391 6392 64116 6448 64581 6487 6515 6519 6785 6900 7124 7167 729920 7355 7357 7364 7368 7841 79143 79147 7915 79644 79709 79796 79868 7991 79944 79947 80055 8050 80896 81562 8398 8399 84197 84342 847 84720 8482 84892 84992 8526 8527 85365 8540 8560 8733 8802 8803 8867 8869 8879 9091 9126 91869 9197 9215 93183 93210 9394 94005 9487 9488 952 9524 9536 960 9993	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:5842	testis seminoma Aliases: Seminoma of testis Seminoma testis testicular Seminoma Pure	ACACA ACE ALPP CD44 CLGN CYP17A1 CYP19A1 CYP1A1 CYP2B6 CYP3A5 CYP3A7 ETNK1 GGT1 HMMR HPGDS ICAM1 IL18R1 L1CAM LDHC LGALS3 LY6K MCFD2 MRC1 PCYT1A PGD PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTEN SLC2A5 SMUG1 SPACA3 STS SULF1 SULF2 UGT1A1	1047 124912 1543 1551 1555 1577 1586 1588 1636 23213 23583 250 2678 27306 31 3161 3383 3897 3948 3958 412 4360 5130 5226 5290 5291 5293 5294 54658 54742 55500 55959 5716 5728 6518 8809 90411 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:9669	senile cataract	CAT CD14 EFNA5 G6PD GALK1 GPX1 HPGDS LSS OGG1 PARP1 PLCD3	113026 142 1946 2539 2584 27306 2876 4047 4968 847 929	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0060823	syndromic X-linked intellectual disability 94 Aliases: MRX94 MRXS29 mental retardation, X-linked 94 syndromic X-linked intellectual disability due to GRIA3 anomalies syndromic X-linked mental retardation 29 syndromic X-linked mental retardation Wu type	ACAT1 ACO2 ACOX1 ACSL4 ALDH5A1 ALG13 ALG14 ARSD B3GALNT2 COG5 CYB5R3 DAG1 DBT DGKK DPAGT1 ECHS1 FKRP FKTN FUCA1 GCK GMPPB HMGCL IL1RAPL1 IMPA1 L1CAM L2HGDH LARGE1 LMAN2L MAN1B1 MBOAT7 MGAT2 MRC1 NAGA NAGLU NANS NDST1 PDHA1 PGAP1 PGAP2 PGAP3 PIGC PIGL PIGO PIGV PIGW PIGY POMGNT1 POMT1 POMT2 PPT1 RFT1 SDHA SLC35A2 SLC35A3 SMC3 SRD5A3 ST3GAL3 ST3GAL5 SUCLG1 TECR TUSC3	10466 10585 11141 11253 139189 148789 1605 1629 1727 1798 1892 199857 2182 2218 23443 2517 2645 27315 284098 29925 29954 3155 3340 3612 38 3897 414 4247 4360 4668 4669 50 51 5160 5279 54187 5538 55624 55650 6389 6487 7355 79143 79147 7915 79644 79868 7991 79944 80055 81562 84720 84992 8802 8869 9126 91869 9215 93210 9487 9524	Homo sapiens (human)	DisGeNET
DOID:8541	Sezary's disease Aliases: Sezary disease Sezary syndrome	ANXA5 CD44 IL18R1 KLRK1 MTAP PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLCG1 PTEN SDC4 SELL SOAT1	142 22914 308 4507 5290 5291 5293 5294 5335 5728 6385 6402 6646 8809 960	Homo sapiens (human)	DisGeNET
DOID:13487	childhood disintegrative disease Aliases: Disintegrative psychosis Heller's syndrome Symbiotic psychosis	ACHE CALR COMT HPGDS	1312 27306 43 811	Homo sapiens (human)	DisGeNET
DOID:14115	toxic shock syndrome Aliases: TSS toxic shock	ACE ENO2 FCGR3B FUT2 HSPG2 MBL2 SELL SLC5A1 TNF	1636 2026 2215 2524 3339 4153 6402 6523 7124	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:10301	parotitis	CALR PIK3CD	5293 811	Homo sapiens (human)	DisGeNET
DOID:10303	sialadenitis Aliases: Sialoadenitis	CALR PIK3CD	5293 811	Homo sapiens (human)	DisGeNET
DOID:2710	sick building syndrome	PNPLA6	10908	Homo sapiens (human)	DisGeNET
DOID:10325	silicosis Aliases: Pneumoconiosis due to silicates Silica pneumoconiosis Silicotic fibrosis of lung silicotuberculosis	ACE CD44 CHIA CPM PTEN PTGS2 SDC2 SELL SFTPD TM7SF2 TNF	1368 1636 27159 5728 5743 6383 6402 6441 7108 7124 960	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:3572	intracranial sinus thrombosis	GPX3 PC SMUG1	23583 2878 5091	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0050127	sinusitis	CHIA LTC4S PLAUR PNP PTGDS SFTPA1 SFTPD ST8SIA4 TLR2 TLR4	27159 4056 4860 5329 5730 6441 653509 7097 7099 7903	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:14501	Sjogren-Larsson syndrome Aliases: FALDH deficiency SLS Sjogren Larsson syndrome Sjogren-Larsson's syndrome fatty acid alcohol oxidoreductase deficiency	ACSL3 ACSL4 ADH5 ALDH3A1 ALDH3A2 ALDH3B1 ALDH3B2 ALOX12B CERS3 EBP ELOVL4 GBA1 HSD17B6 MRC1 NSDHL STS SULT2B1	10682 128 204219 218 2181 2182 221 222 224 242 2629 412 4360 50814 6785 6820 8630	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:8549	chronic ulcer of skin Aliases: Callous ulcer Indolent ulcer	CLEC7A DCN GALNS GBE1 ICAM1 IDH1 IDH2 NCAM1 OCRL OGT PGM3 PIGL PIK3CA PIK3CB PIK3CD	1634 2588 2632 3383 3417 3418 4684 4952 5238 5290 5291 5293 64581 8473 9487	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0050847	sleep apnea	ACE ADIPOQ CYP1A2 CYP2J2 ENOSF1 GNE GNPTAB IDS LEPR LGALS3 NANS PTEN PTGS2	10020 1544 1573 1636 3423 3953 3958 54187 55556 5728 5743 79158 9370	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:0050848	obstructive sleep apnea Aliases: obstructive sleep apnea syndrome	ACE ACSS2 AGRN ALDOA ALOX5 AMY1A AMY1B AMY1C ANXA5 ARSA ATP6AP2 B3GAT1 CEACAM5 CHAT CHI3L1 CHIT1 COMT CSPG4 CYP1A2 CYP2J2 ENOSF1 GAD1 GHRL GNE GNPTAB GPD1 ICAM1 IDS IDUA IL18R1 KL LEP LEPR LGALS3 NANS NGLY1 NT5E PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PLA2G7 PLCB1 PLCB4 PRKAA2 PTEN PTGDS PTGS1 PTGS2 SCD SFTPC SLC17A5 SLC2A4 SLC33A1 SLC35A2 TM7SF2 TNF VCAM1	10020 10159 1048 1103 1116 1118 1312 1464 1544 1573 1636 226 23236 23659 240 2571 26503 27087 276 277 278 2819 308 3383 3423 3425 375790 3952 3953 3958 410 4907 51738 5290 5291 5293 5294 5332 54187 55556 5563 55768 55902 5728 5730 5742 5743 6319 6440 6517 7108 7124 7355 7412 79158 7941 8809 9197 9365	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0060731	congenital central hypoventilation syndrome Aliases: CCHS Ondine curse Ondine syndrome central congenital hypoventilation syndrome congenital central alveolar hypoventilation syndrome	ACE CYP11B1 CYP11B2 CYP1A2 CYP2J2 ENOSF1 GNE GNPTAB IDS LGALS3 NANS PTEN PTGS2 SLC2A10	10020 1544 1573 1584 1585 1636 3423 3958 54187 55556 5728 5743 79158 81031	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:0080302	mixed sleep apnea Aliases: complex sleep apnea	ACE CYP1A2 CYP2J2 ENOSF1 GNE GNPTAB IDS LGALS3 NANS PTEN PTGS2	10020 1544 1573 1636 3423 3958 54187 55556 5728 5743 79158	Homo sapiens (human)	DisGeNET

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