GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Display
results per page.

Clear

Submissions

GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **2526 - 2550** of **7942** in total

« First

‹ Prev

…

98

99

100

101

102

103

104

105

106

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲
DOID:0111110	maturity-onset diabetes of the young type 13 Aliases: MODY type 13 MODY13	KCNJ11	3767	Homo sapiens (human)
DOID:0060283	peeling skin syndrome Aliases: deciduous skin familial continuous skin peeling syndrome keratosis exfoliativa congenita peeling skin disease	BST2 CHST8 GPI KLRB1	2821 3820 64377 684	Homo sapiens (human)
DOID:3074	giant cell glioblastoma Aliases: Monstrocellular sarcoma	ABO ACACA ACACB ACAT1 ACE ACOT7 ACSL5 ACSS2 AGXT AKR1B10 AKR1B1 ALDH1A3 ALDH3A1 ALDH7A1 ALG2 ALOX5 ALPI ALPP ANXA5 ANXA7 APRT ARF4 ARSA ART1 ASAH1 ATP6AP2 ATP6V0A2 B3GAT1 B3GNT5 B4GALNT1 BAAT BCAN BDH2 CALR CANX CAT CBR1 CD109 CD14 CD22 CD248 CD33 CD38 CD44 CD74 CD93 CDH13 CDS1 CEACAM5 CEACAM7 CERS2 CH25H CHAT CHI3L1 CHPT1 CHST15 CHSY1 CLEC18B CLEC5A CMAS CNTN2 CNTN3 CPT1A CPT1C CS CSPG4 CYB5R2 CYP17A1 CYP19A1 CYP1B1 CYP27A1 CYP27B1 CYP2B6 CYP2E1 CYP46A1 DAG1 DBT DCN DEGS1 DGKA DGKI DGKZ DHCR24 DHDDS DLD EBP ECHS1 EFNA2 ELOVL2 ENO1 ENO2 ENPP1 ENPP2 EXTL3 FADS2 FASN FBP1 FDFT1 FDPS FMOD FOLR1 FUT4 G6PC1 GALNT14 GALNT7 GAPDH GAS1 GFPT1 GLB1 GLO1 GLUL GML GOLPH3 GPC1 GPD1 GPI GPNMB GPX3 HACD1 HK1 HK2 HMMR HPGDS HPSE HSD3B7 HSPG2 ICAM1 IDH1 IDH2 IDUA IL18R1 INPP5B INPP5K INPPL1 KL KLRC3 KLRK1 L1CAM L2HGDH LDHA LGALS1 LGALS3 LGALS8 LGALS9 LSS MAN2A1 MCAT ME1 ME2 MGAT1 MGAT5 MICA MMP25 MMUT MPG MRC1 MSLN MTAP NAMPT NANS NCAM1 NDST1 NEIL3 NEU1 NEU3 NEU4 NT5E OCRL OGA OLR1 OPCML PAFAH1B1 PARG PARP1 PARP3 PCYT1A PDIA3 PFKFB2 PFKFB3 PFKFB4 PFKM PGAM1 PGK1 PI4K2A PIK3C2B PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2A PKD1 PKD2 PKM PLA2G4A PLAUR PLCB1 PLCG1 PLD2 PLOD3 PLPP1 PLPP3 PNP POMGNT1 PPT1 PRKAA2 PRNP PRPS1 PSAP PTEN PTGDS PTGS1 PTGS2 RECK RTN4R SDC1 SDC2 SDHA SELP SGMS1 SIGLEC9 SIRT2 SIRT6 SLC2A3 SLC35F1 SLC37A4 SLC3A1 SMUG1 SOAT1 SPHK1 SPHK2 SRGN ST6GAL1 ST8SIA1 ST8SIA4 STS SUCLG1 SULF1 SULF2 SYNJ1 SYNJ2 THEM4 TIGAR TKT TKTL1 TM7SF2 TNFRSF10C TNKS TPI1 TREH TUSC3 TYMP UGCG UGDH UGP2 ULBP1 UMOD UNG VCAM1 VNN2 VTCN1	10039 100507436 1012 10135 10159 10232 1040 10457 1048 10682 10724 10825 10855 10858 1087 1103 1116 11181 11332 117145 126129 129807 135228 1374 142 1431 1464 1545 1555 1571 1586 1588 1593 1594 1605 1606 1629 1634 1636 1718 1738 189 1890 1892 1943 2023 2026 2137 218 2194 220 2203 2222 2224 222553 22856 22914 22918 22933 231 23213 23236 2331 2348 23545 23583 23601 240 248 250 2526 2538 2542 2583 259230 2597 2619 2673 27087 27180 2720 27306 27349 2739 2752 2765 28 2817 2819 2821 2878 2923 29956 308 3098 3099 31 310 3161 32 3339 3340 3383 3417 3418 3425 353 3633 3636 378 38 3823 3897 3939 3956 3958 3964 3965 4047 410 412 4124 417 4199 4200 4245 4249 427 4350 4360 4507 4594 4684 4758 4860 4907 4952 497190 4973 4978 501 5048 5067 5130 51363 51548 5167 5168 51700 51703 51763 51809 5208 5209 5210 5213 5223 5230 5287 5289 5290 5291 5293 5294 5305 5310 5311 5315 5321 5329 5335 5338 54187 54898 55247 55361 5538 5552 55624 5563 55902 55907 55959 5621 5631 5660 56848 56898 56994 570 57016 57103 57124 5728 5730 5742 5743 6382 63827 6383 6389 6403 64083 64386 6480 6489 65078 6515 6519 6646 6900 7086 7108 7167 7357 7358 7360 7369 7374 7412 7903 79623 79679 7991 79944 79947 80270 80329 811 821 8277 84002 8434 847 8505 8525 85365 8560 8611 8613 8658 873 8794 8802 8809 8867 8871 8875 8877 8985 9023 9162 9200 929 933 9365 9415 945 952 960 972	Homo sapiens (human)
DOID:0110676	congenital myasthenic syndrome 13 Aliases: CMS13 CMSTA2 congenital myasthenic syndrome 13 with tubular aggregates congenital myasthenic syndrome with tubular aggregates 2	DPAGT1	1798	Homo sapiens (human)
DOID:0110428	dilated cardiomyopathy 1AA Aliases: CMD1AA dilated cardiomyopathy 1AA with or without left ventricular noncompaction	ACADVL ACE BDH1 CHKB CPT2 DAG1 DOLK FASN FKRP FKTN GLB1 GPX1 HACD1 HADH HADHA HADHB HJV HMGCL HPRT1 LDHA LGALS3 LPL MDH1 MICA MTM1 NAMPT NCAM1 NDUFAB1 PCYT1A PGM1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 POMT2 RENBP SDHA SDHD SLC2A10 SLC2A4	100507436 10135 1120 1376 148738 1605 1636 2194 2218 22845 2720 2876 29954 3030 3032 3033 3155 3251 37 3939 3958 4023 4190 4534 4684 4706 5130 5236 5290 5291 5293 5294 5973 622 6389 6392 6517 79147 7941 81031 9200	Homo sapiens (human)
DOID:0080072	intestinal pseudo-obstruction Aliases: Chronic intestinal pseudo-obstruction neuronal intestinal dysplasia	PTEN	5728	Homo sapiens (human)
DOID:0070029	ITM2B-related cerebral amyloid angiopathy 1 Aliases: Cerebral Amyloid Angiopathy, British Type FBD Familial British Dementia Presenile Dementia with Spastic Ataxia	GPC1 PRNP	2817 5621	Homo sapiens (human)
DOID:0110403	retinitis pigmentosa 13 Aliases: RP13	PAFAH1B1	5048	Homo sapiens (human)
DOID:9074	systemic lupus erythematosus Aliases: Lupus Erythematosus, systemic SLE - Lupus Erythematosus, systemic disseminated lupus erythematosus	ACACA ACE ACSL4 ACSL5 AKR1C4 ALG1 ANXA5 APRT ARSA ARSF BCKDHB BDH2 BST2 CALR CAT CD14 CD1D CD22 CD33 CD38 CD44 CD48 CD72 CD74 CDH13 CEPT1 CHST12 CLEC16A CLEC7A CNTN6 COG6 COMT CYP19A1 CYP1A1 CYP21A2 CYP24A1 CYP2B6 CYP2C19 CYP2E1 CYP3A5 DAG1 DGAT1 DGKQ DLAT EFNA2 EFNA5 ENO1 EPHX2 FCGR3B FCN2 FCN3 FH FUT2 GALC GCK GLO1 GPI HPGDS HPRT1 HSD11B1 HSD17B6 HSPG2 ICAM1 ICAM5 IL18R1 IL18RAP IL1R1 IL1RAP INPP5D KLRB1 KLRC1 KLRD1 KLRK1 L1CAM LCT LGALS1 LGALS3 LGALS8 LGALS9 LYZ MAN2A1 MASP1 MASP2 MBD4 MBL2 MDGA2 MGAT5 MICA MRC1 MTMR3 NCAM1 NEU1 OGG1 PARP1 PC PDHX PGK1 PGM1 PIGF PIK3C2A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PLA2R1 PLB1 PLD2 PLD4 PNP PRKAA2 PRPS2 PTEN PTGDS PTGS1 PTGS2 RECK RENBP SCD5 SDC1 SDC2 SELE SELL SELP SEMA7A SFTPD SGMS1 SIGLEC12 SIGLEC1 SIGLEC5 SIGLEC6 SLC2A4 SLC39A8 SMPD1 SMUG1 SOAT1 SPHK2 ST8SIA4 TNF TNFRSF10C TPI1 UMOD VCAM1 VTCN1	100507436 1012 10390 10747 1109 122618 1312 142 151056 1543 1555 1557 1571 1577 1588 1589 1591 1605 1609 161357 1636 1737 1943 1946 2023 2053 2182 2215 2220 2271 22914 22925 23274 23583 2524 2581 259230 2645 27255 27306 2739 2821 308 31 3251 3290 3339 3383 353 3554 3556 3635 3820 3821 3824 3897 3938 3956 3958 3964 3965 4069 410 4124 4153 416 4249 4360 4684 4758 4860 4968 5091 51703 5230 5236 5281 5286 5290 5291 5293 5294 5320 5338 55501 5563 56052 5634 5648 56848 56898 5728 5730 5742 5743 57511 594 5973 6382 6383 6401 6402 6403 64116 6441 64581 6517 6609 6614 6646 684 7087 7124 7167 7369 7412 7903 79679 79966 8050 811 8434 847 8482 8547 8630 8694 8778 8794 8807 8809 8897 8930 89858 912 929 933 945 946 952 960 962 971 972	Homo sapiens (human)
DOID:986	alopecia areata Aliases: Circumscribed alopecia	ABO ACE CLEC16A ICAM1 LGALS8 SOAT1	1636 23274 28 3383 3964 6646	Homo sapiens (human)
DOID:0070226	progressive familial intrahepatic cholestasis 1 Aliases: FIC1 deficiency PFIC1	ABO GGT1 HSD3B7 NAGLU OGA	10724 2678 28 4669 80270	Homo sapiens (human)
DOID:0111068	congenital bile acid synthesis defect 4 Aliases: CBAS4 intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid trihydroxycoprostanic acid in bile	AMACR HSD17B4	23600 3295	Homo sapiens (human)
DOID:0110586	autosomal dominant nonsyndromic deafness 65 Aliases: DFNA65 autosomal dominant deafness 65	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:3178	skin papilloma Aliases: cutaneous papilloma papilloma of skin	AMACR CD44 CYP24A1 G6PD GALK1 GLB1 GPC3 HPSE ICAM1 LGALS3 LGALS9 MTAP NSDHL PARP1 PIK3CA PKD1 PKM PLA2G6 PLCB4 PTEN PTGS2 RECK SDHB SDHC SDHD SIRT6 STS TLR2 VCAN	10855 142 1462 1591 23600 2539 2584 2719 2720 3383 3958 3965 412 4507 50814 51548 5290 5310 5315 5332 5728 5743 6390 6391 6392 7097 8398 8434 960	Homo sapiens (human)
DOID:9768	heart aneurysm Aliases: cardiac aneurysm	SMUG1	23583	Homo sapiens (human)
DOID:5605	breast medullary carcinoma Aliases: Medullary breast carcinoma with lymphoid Stroma	MGLL	11343	Homo sapiens (human)
DOID:1762	cheilitis	CLEC7A OCRL	4952 64581	Homo sapiens (human)
DOID:0111453	2-aminoadipic 2-oxoadipic aciduria Aliases: AMOXAD alpha-aminoadipic aciduria	DHTKD1	55526	Homo sapiens (human)
DOID:0050156	idiopathic pulmonary fibrosis Aliases: FIBROCYSTIC PULMONARY DYSPLASIA IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL cryptogenic fibrosing alveolitis	ACE AKT1 ALOX5 ALPI ALPP ANXA5 ATP6AP2 B3GAT3 CD248 CD55 CEACAM5 CEACAM7 CEL CEMIP CHI3L1 CTSA CYP2C9 DCN ELOVL6 ENPP2 FCGR3B FOLR2 GGT1 GLB1 HK2 HS6ST1 HS6ST2 ICAM1 IL18R1 IL1RL1 KL KLRK1 L1CAM LCLAT1 LDHA LGALS1 LGALS3 LTA4H MICA MPG MRC1 NEU1 NT5E PARP1 PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKD2 PRKAA2 PTEN PTGS1 PTGS2 SDC1 SDC2 SDC4 SEMA7A SFTPA1 SFTPA2 SFTPC SFTPD SHMT2 SIRT6 SLC27A5 SLC2A10 SLC2A5 SMUG1 SOAT1 SPHK1 SULF2 TM7SF2 VCAM1 VCAN	100507436 10159 1048 1056 1087 10998 1116 142 1462 1559 1604 1634 1636 207 2215 22914 2350 23583 240 248 250 253558 26229 2678 2720 308 3099 3383 3897 3939 3956 3958 4048 4350 4360 4758 4907 51548 5168 5290 5291 5293 5294 5310 5311 5476 5563 55959 57124 57214 5728 5742 5743 6382 6383 6385 6440 6441 6472 6518 653509 6646 7108 729238 7412 79071 81031 83666 8482 8809 8877 90161 9173 9365 9394	Homo sapiens (human)
DOID:670	amphetamine abuse	ACHE ACSL6 CD55 CDH13 COMT GAD1 GAD2 HS3ST4 LARGE1 NPY1R	1012 1312 1604 23305 2571 2572 43 4886 9215 9951	Homo sapiens (human)
DOID:0060698	hyperekplexia 3 Aliases: HKPX3	PRNP	5621	Homo sapiens (human)
DOID:9220	central sleep apnea Aliases: primary central sleep apnea	AGRN ALDH2 ANXA5 CAT CHAT COMT CYP3A5 INPP5E OLR1 PCYT1A PLCB4 PRPS1 PSAP SLC35A2	1103 1312 1577 217 308 375790 4973 5130 5332 5631 5660 56623 7355 847	Homo sapiens (human)
DOID:0110570	autosomal dominant nonsyndromic deafness 47 Aliases: DFNA47 autosomal dominant deafness 47	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:0050432	Asperger syndrome	ARSD SLC25A12	414 8604	Homo sapiens (human)
DOID:686	liver carcinoma Aliases: Liver and Intrahepatic bile duct carcinoma	ACACA ACADL ACHE ACOT7 ACOX1 ACSL1 ACSM3 ACSS2 AKR1B10 AKR1C1 AKR1C2 AKR1C3 AKR1C4 ALDH2 ALDH7A1 ALPP ANXA5 ANXA7 ATRNL1 B3GAT3 CD44 CEACAM5 CEACAM7 CERS4 CHI3L1 CLEC7A COMT CPT1A CRYL1 CYP17A1 CYP2C9 DCN DLD ECHS1 ELOVL6 ENO1 FASN FBP1 FOLR2 G6PD GALNT14 GCK GGT1 GNPAT GOLPH3 GPC3 HK1 HK2 HMGCS2 HPGDS HSD17B4 HSPG2 ICAM1 IDH1 IDH2 IDUA IGF2R KLRC1 KLRK1 LGALS1 LGALS9 MICA MRC1 MTMR14 OGT PARG PARP1 PCK1 PCK2 PCYT1B PEMT PFKM PGK1 PGM5 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLA2G6 PNPLA3 PRKAA2 PSMD10 PTEN PTGS2 RGN RPE RPIA RTN4R SCD SELP SHMT2 SIRT4 SIRT6 SLC17A5 SLC2A4 SMPD1 SMUG1 SOAT1 SORD SPHK1 SPHK2 SRD5A2 STS SULF1 SULF2 TIGAR UGT1A1 UGT2B7 VCAM1 VCAN	100507436 10400 1048 1087 1109 1116 11332 1312 1374 142 1462 1559 1586 1634 1645 1646 1738 1892 2023 217 2180 2194 2203 22914 22934 23213 23409 2350 23583 250 2539 26033 26229 2645 26503 2678 2719 27306 308 3098 3099 31 310 3158 3295 33 3339 3383 3417 3418 3425 3482 3821 3956 3965 412 43 4360 501 51 5105 5106 51084 51548 5213 5230 5239 5290 5291 5293 5294 5315 54658 5563 55902 55959 56848 57016 57103 5716 5728 5743 6120 6296 6319 6403 64083 64419 64581 6472 65078 6517 6609 6646 6652 6716 7364 7412 79071 79603 79623 80339 8398 8443 8473 8505 8644 8877 9104 9468 960	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements