GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

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), 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 **826 - 850** of **7942** in total

« First

‹ Prev

…

30

31

32

33

34

35

36

37

38

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:13097	intracranial arteriosclerosis	ACE ACHE IMPA1	1636 3612 43	Homo sapiens (human)	DisGeNET DisGeNET
DOID:12720	cerebral atherosclerosis	ACE ACHE IMPA1	1636 3612 43	Homo sapiens (human)	DisGeNET 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:7587	supraglottis squamous cell carcinoma Aliases: Epidermoid carcinoma of the Supraglottis	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:1577	limited scleroderma Aliases: Limited cutaneous systemic sclerosis systemic sclerosis, limited	CD22	933	Homo sapiens (human)	DisGeNET
DOID:4784	immune-complex glomerulonephritis Aliases: Immune Complex Glomerulonephritis	LGALS9	3965	Homo sapiens (human)	DisGeNET
DOID:0050836	focal dystonia	ALDH5A1 ARSG PLA2G6	22901 7915 8398	Homo sapiens (human)	DisGeNET
DOID:1584	acute chest syndrome Aliases: acute chest syndrome in sickle cell disease	ABO ACACA ACACB ACE ACSL5 ACSL6 ACSS2 ALDH2 ALOX5 ARSA CD14 CD44 CHI3L1 CYP1A1 CYP2C19 CYP3A4 CYP3A5 ELOVL2 EPHX2 FADS1 FASN FCGR3B G6PD GALNT4 GCK HYAL2 ICAM1 L1CAM LCAT LGALS3 LIPA LIPG LPL OGG1 OLR1 PCYT1A PLA2G15 PLA2G2A PLA2G4A PLA2G6 PLA2G7 PLB1 PLCB4 PTGS1 PTGS2 SELE SELL SELP SLC39A8 SMUG1 VCAM1	1116 151056 1543 1557 1576 1577 1636 2053 217 2194 2215 23305 23583 23659 240 2539 2645 28 31 32 3383 3897 3931 3958 3988 3992 4023 410 4968 4973 5130 51703 5320 5321 5332 54898 55902 5742 5743 6401 6402 6403 64116 7412 7941 8398 8692 8693 929 9388 960	Homo sapiens (human)	DisGeNET
DOID:1920	hyperuricemia Aliases: Blood urate raized uricacidemia	ACAT1 ALDH2 ALDOB CAT DPEP1 FBP1 G6PC1 HAS2 HMGCL HPRT1 INS KHK PC PFKM PLA2G7 PNP PRPS1 SLC37A4 UMOD	1800 217 2203 229 2538 2542 3037 3155 3251 3630 3795 38 4860 5091 5213 5631 7369 7941 847	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:3525	middle cerebral artery infarction	ACACA ACE AGXT ALDH2 ALOX5 BAD BCAN CAT CD14 CHAT CHI3L1 CYP19A1 CYP2C8 CYP2E1 CYP2J2 ENO1 EPHX2 G6PD GAD1 GAD2 GAPDH GHRL GLUL GSK3B HAS2 HJV HK2 HPRT1 ICAM1 KL LDHA LGALS3 LPIN1 LYPD5 MAG MGLL NAMPT NCAM1 OGG1 PARP1 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G4A PLD1 PRKAA2 PTEN PTGS2 RGMA RGMB SFTPD SIRT2 SLC2A1 SLC2A3 SLC5A1 SMUG1 SPHK2 STS TM7SF2 TNF UMOD UPP1	10135 1103 1116 11343 142 148738 1558 1571 1573 1588 1636 189 2023 2053 217 22933 23175 23583 240 2539 2571 2572 2597 2752 284348 285704 2932 3037 3099 31 3251 3383 3939 3958 4099 412 4684 4968 51738 5290 5291 5293 5294 5321 5337 5563 56848 56963 572 5728 5743 63827 6441 6513 6515 6523 7108 7124 7369 7378 847 929 9365	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:0090016	chromosome 5q deletion syndrome Aliases: 5q- syndrome, refractory macrocytic anemia due to 5q deletion myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality	ANXA5 CD14 CD74 HMMR	308 3161 929 972	Homo sapiens (human)	DisGeNET DisGeNET
DOID:0050445	X-linked dominant hypophosphatemic rickets Aliases: Hypophosphatemia, Vitamin D-Resistant Rickets Vitamin D-Resistant Rickets, X-Linked X-linked hypophosphatemia hypophosphatemic rickets X-linked dominant	CYP24A1 CYP27B1 ENPP1 KL L1CAM SFTPA1 SLC2A2	1591 1594 3897 5167 6514 653509 9365	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:9191	diabetic macular edema	CD14 CHI3L1 GAL3ST1 HK1 ICAM1 LGALS1 PLA2G7 RPE SLC35A1	10559 1116 3098 3383 3956 6120 7941 929 9514	Homo sapiens (human)	DisGeNET
DOID:8946	severe nonproliferative diabetic retinopathy Aliases: High risk non proliferative diabetic retinopathy Severe NPDR	DPEP1	1800	Homo sapiens (human)	DisGeNET
DOID:9820	central gyrate choroidal dystrophy Aliases: Choroidal dystrophy, serpiginous	ACE	1636	Homo sapiens (human)	DisGeNET
DOID:12638	hypertrophic pyloric stenosis Aliases: congenital hypertrophic pyloric stenosis congenital or infantile stricture of pylorus	UGT1A1	54658	Homo sapiens (human)	DisGeNET
DOID:0080028	spondyloepimetaphyseal dysplasia, Strudwick type	PCYT1A	5130	Homo sapiens (human)	DisGeNET
DOID:4306	radiculopathy Aliases: pinched nerve	APRT TNF	353 7124	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:3451	skin carcinoma Aliases: carcinoma of skin	CYP1A1 CYP27A1 CYP27B1 HPGDS HSD11B2 INPP5K MICA MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PTGS2	100507436 1543 1593 1594 27306 3291 4360 51763 5290 5291 5293 5294 5743	Homo sapiens (human)	DisGeNET
DOID:120	female reproductive organ cancer Aliases: female reproductive cancer malignant Gynecologic tumor malignant neoplasm of female genital organ	AMT HPGDS MRC1 PIK3CA UGT1A10 UGT1A1 UGT1A4 UGT1A6 UGT1A7 UGT1A8	27306 275 4360 5290 54575 54576 54577 54578 54657 54658	Homo sapiens (human)	DisGeNET
DOID:1520	colon carcinoma Aliases: Colonic carcinoma carcinoma of colon	ACACA ACAT1 ACE ACLY ACSBG1 ACSL1 ACSL4 ACSS2 ADH1B ADH1C AGL AKR1B10 AKR1B1 ALDH1A3 ALDH1B1 ALDH2 ALDH3A1 ALDH7A1 ALOX15 ALOX5 ALPP AMACR ANXA5 APRT ARSA ART1 ASAH1 ATRNL1 B3GALT5 B3GNT6 B3GNT7 B3GNT8 B3GNTL1 B4GALNT3 BAAT BPHL BRAF C1GALT1 CA4 CALR CAT CBR1 CD248 CD44 CDH13 CEACAM5 CEACAM6 CEACAM7 CEMIP CHAT CHGA CHI3L1 CHKA CHPT1 CHST4 COMT CSGALNACT1 CTBS CYB5R1 CYP19A1 CYP1A1 CYP1A2 CYP24A1 CYP27B1 CYP2E1 CYP2R1 CYP3A4 CYP4F3 CYP7A1 CYP7B1 DAG1 DCN DGKB DGKE DGKZ DHCR24 DHCR7 DHDDS DLD DPEP1 EBP EFNA1 ENO1 ENPP3 ENPP7 FADS1 FASN FBP1 FH FMOD FOLR1 FUT1 FUT2 FUT3 FUT4 FUT6 FUT7 G6PD GALNT4 GALNT6 GAPDH GCNT2 GCNT3 GLB1 GLO1 GLTP GMDS GOLPH3 GPC1 GPI GPLD1 GPX1 GPX2 GPX3 GUSB HAS3 HEXB HK2 HMGCS1 HMGCS2 HMMR HPGDS HPRT1 HPSE HSD11B2 HSD17B4 HSD17B7 HSPG2 HYAL2 ICAM1 IDH1 IDUA IGF2R IL1R1 IMPA1 INPP4B INPP5D INPPL1 ISYNA1 KL KLRK1 L1CAM LDHA LDHB LGALS12 LGALS1 LGALS3 LGALS4 LGALS9 LIPC LPIN1 LYNX1 LYPD5 MACROD2 MBD4 MBL2 ME1 MGLL MICA MMP25 MMUT MRC1 MTAP MTM1 MTMR3 MUTYH NAMPT NEU3 NTNG1 OGA OGG1 OLR1 PARG PARP1 PCYT1A PCYT1B PFKFB3 PGK1 PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1A PKM PLA2G10 PLA2G15 PLA2G1B PLA2G2A PLA2G2D PLA2G3 PLA2G4A PLA2G7 PLAUR PLB1 PLCG1 PLD2 PLD4 PLEKHA8 PNP PNPLA2 POGLUT1 PRKAA2 PSMD10 PTEN PTGDS PTGES PTGIS PTGS1 PTGS2 RECK REG1B RENBP RGN RPIA RPN2 SCD SDC1 SDC2 SDC4 SELE SELL SELP SGMS2 SGPL1 SHMT1 SHMT2 SIGLEC7 SIRT2 SIRT6 SLC17A5 SLC26A2 SLC2A2 SLC2A3 SLC2A4 SLC2A5 SLC35A2 SLC3A1 SMC3 SMPD1 SMUG1 SOAT1 SPHK1 SPHK2 SRGN ST3GAL4 ST6GAL1 ST6GALNAC1 STT3A SULT1E1 SYNJ2 TDG TKT TKTL1 TKTL2 TM7SF2 TMED3 TMED9 TNKS TUSC3 TYMP UGT1A1 UGT1A6 UGT1A7 UGT1A9 UGT2B17 ULBP2 UNG VCAM1 VCAN VNN1	100507436 1012 10135 10164 10317 1048 10682 10724 10825 10855 1087 1103 1113 1116 1119 11226 11343 120227 122618 125 126 1312 140733 142 1462 146712 1486 151056 1543 1544 1571 1576 1581 1588 1591 1594 1605 1607 1634 1636 166929 1717 1718 1738 178 1800 1836 1890 192134 1942 2023 217 218 2180 2182 219 2194 220 2203 2271 22854 22914 22933 22934 231 23175 23205 2331 23423 2348 23583 23600 23659 240 246 250 2523 2524 2525 2526 2528 2529 2539 2597 26033 26279 26503 2651 27036 2720 27306 2739 2762 2817 2821 2822 283358 284348 2876 2877 2878 2990 3038 3074 308 3099 31 3157 3158 3161 3251 3291 3295 3339 3383 339221 3417 3425 3482 353 3554 3612 3635 3636 3703 374907 38 3897 3939 3945 3956 3958 3960 3965 3990 3992 4051 410 4153 417 4199 427 4360 4507 4534 4594 4595 4680 47 4860 4968 4973 501 50487 51228 5130 51477 51478 51548 5169 51706 5209 5230 5289 5290 5291 5293 5294 5315 5319 5320 5321 5329 5335 5338 54577 54578 54600 54658 54732 5552 5563 55790 55808 55902 56848 56913 56983 56994 570 57016 57104 57124 5716 57214 5728 5730 5740 5742 5743 5968 5973 6185 6319 6382 6383 6385 6401 6402 6403 64083 64386 6470 6472 6480 6484 6514 6515 6517 6518 6519 66004 6609 6646 670 673 6783 6996 7086 7108 7355 7367 7374 7412 762 7941 7991 79947 80328 811 8277 8394 8399 84076 8434 847 84725 8505 8525 8526 85329 8658 8692 8693 873 8821 8871 8876 8877 8879 8897 8930 9104 9126 9245 93010 9365 9420 9468 9536 960	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:12712	nephronophthisis Aliases: medullary cystic disease medullary cystic kidney	ACE AGXT ALDH3A2 LGALS1 MLYCD UMOD	1636 189 224 23417 3956 7369	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0050857	Perrault syndrome	HSD17B4	3295	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:2602	chondroma Aliases: central Chondroma	AMACR EXT1 IDH1 IDH2 PIGA PIK3CA PIK3CB PIK3CD PIK3CG SDHB SMUG1	2131 23583 23600 3417 3418 5277 5290 5291 5293 5294 6390	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:5442	eccrine acrospiroma Aliases: Eccrine hidradenoma Eccrine hidradenoma of skin Poroma	CEACAM5	1048	Homo sapiens (human)	DisGeNET DisGeNET

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