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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 **3526 - 3550** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:850	lung disease	ABO ACE ACLY ACOD1 ALDH2 ALDH7A1 ALOX5 APEX1 ARSA ATP6V0A2 BST1 CALR CAT CD14 CD1D CD44 CD55 CEACAM5 CEACAM6 CEACAM7 CEL CHGA CHI3L1 CHIT1 CNTN2 CYP1A1 CYP27B1 CYP2C9 DCN DGKA DHCR24 DLD ENO1 ENO2 FCN2 FUT3 GLA GOLPH3 GPX1 GPX3 HMMR HPGDS ICAM1 IGF2R IL18R1 IL1RL1 ISYNA1 LDHC LGALS3 LGALS9 LTC4S MBL2 NAMPT NTM PARP9 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PLCB3 PTEN PTGS1 PTGS2 RECK RENBP RGMA SFTPA1 SFTPA2 SFTPC SFTPD SLC27A5 SMUG1 SPHK2 TLR2 TLR4 TNF VCAN	10135 1048 1056 1087 10998 1113 1116 1118 1462 1543 1559 1594 1604 1606 1634 1636 1718 1738 2023 2026 217 2220 23545 23583 240 2525 2717 27306 28 2876 2878 3161 328 3383 3482 3948 3958 3965 4056 410 4153 4680 47 501 50863 51477 5290 5291 5293 5294 5320 5331 56848 56963 5728 5742 5743 5973 64083 6440 6441 653509 683 6900 7097 7099 7124 729238 730249 811 83666 8434 847 8809 912 9173 929 960	Homo sapiens (human)
DOID:255	hemangioma	C1GALT1C1 CALR CD14 CTSA DPM1 GAS1 GNPTAB GPC6 HSD17B2 IDH1 IDH2 IGF2R IL18R1 LGALS9 MAG MTM1 MTMR14 PIGF PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PNPLA2 PNPLA6 PTEN SDHB SDHC SDHD SLC2A1	10082 10908 2619 29071 3294 3417 3418 3482 3965 4099 4534 5281 5290 5291 5293 5294 5310 5476 57104 5728 6390 6391 6392 64419 6513 79158 811 8809 8813 929	Homo sapiens (human)
DOID:0110178	Charcot-Marie-Tooth disease axonal type 2V Aliases: CMT2V Charcot-Marie-Tooth neuropathy type 2V autosomal dominant Charcot-Marie-Tooth disease type 2V autosomal dominant axonal Charcot-Marie-Tooth disease type 2V	NAGLU	4669	Homo sapiens (human)
DOID:6901	familiar ovarian carcinoma	PARP1 PIK3CA	142 5290	Homo sapiens (human)
DOID:0080564	congenital disorder of glycosylation Il Aliases: congenital disorder of glycosylation 1l	alg9	393598	Danio rerio (zebrafish)
DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2 Aliases: CVPT2	ACADVL ACE CALR CHPT1 FKRP FUT1 GOLPH3 GYG1 PTGS2 SCD	1636 2523 2992 37 56994 5743 6319 64083 79147 811	Homo sapiens (human)
DOID:9993	hypoglycemia Aliases: Hypoglycaemia	Akt2 Gck Ppp1r3a	103988 11652 140491	Mus musculus (house mouse)
DOID:0050814	temtamy preaxial brachydactyly syndrome Aliases: PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE	CHSY1 TGDS	22856 23483	Homo sapiens (human)
DOID:4692	endophthalmitis	Tnf	21926	Mus musculus (house mouse)
DOID:783	end stage renal disease Aliases: end stage renal failure end-stage kidney disease	Adipoq Cpt1a Enpp1 Kl Lep Pgf Tlr2 Tlr4 Tnf Ucp2	11450 12894 16591 16846 18605 18654 21898 21926 22228 24088	Mus musculus (house mouse)
DOID:0080071	mucolipidosis III alpha/beta Aliases: mucolipidosis III pseudo-Hurler polydystrophy	GLB1 GNPTAB GNPTG NAGPA OGA	10724 2720 51172 79158 84572	Homo sapiens (human)
DOID:3372	chondroblastic osteosarcoma Aliases: chondrosarcomatous Osteogenic sarcoma	IDH1	3417	Homo sapiens (human)
DOID:1825	childhood absence epilepsy Aliases: petit mal seizure pyknolepsy	ALPI ALPP CACNA2D2 CANX NPY1R PDIA3 PIGO PLCB4 SLC2A1	248 250 2923 4886 5332 6513 821 84720 9254	Homo sapiens (human)
DOID:13258	typhoid fever Aliases: Typhoid	ABO CD38 TNF	28 7124 952	Homo sapiens (human)
DOID:784	chronic kidney disease Aliases: CKD CRF chronic kidney failure chronic renal disease chronic renal failure syndrome renal failure - chronic	ABO ACACA ACADL ACADS ACAT1 ACE ACHE ACLY ACSBG1 ACSM3 ACSS2 AGXT AKR1B1 ALDH2 ALDOB AMACR ANXA5 APRT ARSA ATP6AP2 B3GAT1 CAT CBR1 CD14 CD177 CD248 CD55 CDH13 CERS2 CERS4 CHGA CHI3L1 CLEC16A CMAS CNTN3 COL9A2 COMT CPT1A CPT2 CYP11B2 CYP1A1 CYP1A2 CYP24A1 CYP27B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP3A4 CYP3A5 DDOST DGAT1 DGAT2 DHCR24 DPEP1 ENO1 ENPP1 EPHX2 EXTL2 FADS1 FADS2 FAR2 FASN FCGR3B G6PC1 GAD1 GALNT3 GFPT2 GGT1 GLA GLB1 GPX1 GPX3 GRHPR HJV HOGA1 HPGDS HPSE HSD11B1 HSD11B2 ICAM1 IGF2R KL LCAT LEPR LGALS3 LIPC LPIN1 LPL MANBA MBL2 MBOAT7 MICA MPI MTM1 NAGLU NAMPT OCRL OGA OGG1 OLR1 PARP1 PCYT1A PIK3C3 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1B PKD1 PKD2 PLA2G10 PLA2G15 PLA2G2A PLA2R1 PLB1 PLCE1 PLD1 PLD2 PNPLA3 PRKAA2 PRNP PTGDS PTGES PTGS1 PTGS2 RBP4 RENBP RGMA RPN1 SDC1 SELE SELL SELP SFTPA1 SHMT1 SIRT6 SLC17A5 SLC2A4 SLC33A1 SLC3A1 SMPD3 SMUG1 SPHK2 ST8SIA4 STS TALDO1 TKT UMOD VCAM1 VCAN VNN1 XYLT2	100507436 1012 10135 10159 10724 10855 1113 1116 112817 1298 1312 1374 1376 142 1462 148738 151056 1543 1544 1555 1557 1558 1559 1576 1577 1585 1591 1594 1604 1636 1650 1718 1800 189 2023 2053 2135 217 2194 2215 229 22925 231 23175 23205 23274 23583 23600 23659 2538 2571 2591 26503 2678 27087 2717 2720 27306 28 2876 2878 29956 308 31 3290 3291 33 3383 3482 35 353 38 3931 3953 3958 3990 3992 4023 410 412 4126 4153 43 4351 4534 4669 47 4952 4968 4973 5067 51196 5130 51548 5167 5289 5290 5291 5293 5294 5310 5311 5320 5337 5338 55512 5563 55711 55902 55907 5621 56848 56963 57124 57126 5730 5742 5743 5950 5973 6184 6296 6382 6401 6402 6403 64132 6470 6517 6519 653509 6888 7086 7369 7412 7903 79143 79603 80339 8395 8399 84649 847 8694 873 8876 9197 929 9365 9380 9415 9536 9945	Homo sapiens (human)
DOID:0070253	congenital disorder of glycosylation type IIa Aliases: Alkuraya syndrome CDG IIa CDG2A CDGIIa CDGS2 carbohydrate-deficient glycoprotein syndrome, type II congenital disorder of glycosylation, type IIa mental retardation, growth retardation, prominent columella, and open mouth	gly-20	179562	Caenorhabditis elegans
DOID:2634	cystadenoma Aliases: Cystoma	CHST3 GOLPH3 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SFTPC TNFRSF10C	5290 5291 5293 5294 5728 64083 6440 8794 9469	Homo sapiens (human)
DOID:11555	Fuchs' endothelial dystrophy Aliases: FCED Fuchs' corneal dystrophy Fuchs' endothelial corneal dystrophy	NEIL1 PIK3CA PIK3CB PIK3CD PIK3CG	5290 5291 5293 5294 79661	Homo sapiens (human)
DOID:1080	filariasis Aliases: disease due to superfamily Filarioidea	ABO CHIT1 GLB1 LGALS2 MBL2	1118 2720 28 3957 4153	Homo sapiens (human)
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	c1galt1c1	448225	Xenopus tropicalis (tropical clawed frog)
DOID:2739	Gilbert syndrome Aliases: Constitutional hyperbilirubinemia Gilbert's disease Gilbert's syndrome Gilbert-Meulengracht syndrome hereditary nonhemolytic jaundice	ABO AKR1D1 ALDOB AMACR COG6 CYP2B6 ENO2 FH G6PD HK1 HSD3B7 LPL NT5E PGK1 PRKAA2 SELP SLC17A5 SLC35A2 UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UMPS XYLT2	1555 2026 2271 229 23600 2539 26503 28 3098 4023 4907 5230 54575 54576 54577 54578 54579 54600 54657 54658 54659 5563 56886 57511 6403 64132 6718 7355 7372 80270	Homo sapiens (human)
DOID:7998	hyperthyroidism Aliases: overactive thyroid	cts-1 ugt-62	175591 176437	Caenorhabditis elegans
DOID:2571	Langerhans-cell histiocytosis Aliases: Histiocytosis X Langerhan's cell histiocytosis Langerhans cell granulomatosis Letterer-Siwe disease Letterer-Siwe disease involving intra-abdominal lymph nodes Letterer-Siwe disease involving intrapelvic lymph nodes Letterer-Siwe disease involving intrathoracic lymph nodes Letterer-Siwe disease involving lymph nodes of axilla and upper limb Letterer-Siwe disease involving lymph nodes of head, face and neck Letterer-Siwe disease involving lymph nodes of head, face, and neck Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb Letterer-Siwe disease involving lymph nodes of multiple sites Letterer-Siwe disease involving spleen Letterer-Siwe disease of intra-abdominal lymph nodes Letterer-Siwe disease of intrapelvic lymph nodes Letterer-Siwe disease of intrathoracic lymph nodes Letterer-Siwe disease of lymph nodes of axilla and upper limb Letterer-Siwe disease of lymph nodes of axilla and/or upper limb Letterer-Siwe disease of lymph nodes of head, face and neck Letterer-Siwe disease of lymph nodes of head, face and/or neck Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb Letterer-Siwe disease of lymph nodes of inguinal region and lower limb Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb Letterer-Siwe disease of lymph nodes of multiple sites Letterer-Siwe disease of spleen	ACAA1 ACACA ACE ACSBG1 AKR1A1 AKR1C1 AKR1C3 ALPP AMACR ANXA5 APRT ATRNL1 BRAF CAT CD14 CD22 CD33 CD38 CD44 CD55 CDH13 CFC1 COMT CYP17A1 CYP1A1 CYP1B1 CYP24A1 CYP27B1 CYP2B6 CYP2C9 CYP2E1 EPHX2 FCGR3B FCN2 FH G6PD GBA1 GPX1 HPGDS ICAM1 IDH1 IDH2 KLRK1 LGALS1 LGALS3 LYZ MASP2 MCAT MTAP NCAM1 NTHL1 OGG1 PAFAH1B1 PARP1 PC PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGS2 SELE SELL SHMT1 SHMT2 SLC35B2 SMUG1 SOAT1 TMEM260 VCAM1 VTCN1	1012 10327 10747 1312 142 1543 1545 1555 1559 1571 1586 1591 1594 1604 1636 1645 2053 2215 2220 2271 22914 23205 23583 23600 250 2539 26033 2629 27306 27349 2876 30 308 31 3383 3417 3418 347734 353 3956 3958 4069 4507 4684 4913 4968 5048 5091 5290 5291 5293 5294 54916 55997 5728 5743 6401 6402 6470 6472 6646 673 7412 79679 847 8644 929 933 945 952 960	Homo sapiens (human)
DOID:7188	autoimmune thyroiditis Aliases: Chronic Lymphocytic Thyroiditis Hashimoto thyroiditis Hashimoto's Disease Hashimoto's syndrome Hashimoto's thyroiditis Lymphocytic Thyroiditis	CD14 CD38 CYP19A1 CYP21A2 CYP27B1 DAG1 FUT2 GAD1 GAD2 GLUL GPX3 ICAM1 IL18R1 IL18RAP IL1RL1 LGALS3 MBL2 NCAM1 NT5E PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLCG2 PTEN PTGDS PTGS2 RENBP SOAT1	1588 1589 1594 1605 2524 2571 2572 2752 2878 3383 3958 4153 4684 4907 5130 5290 5291 5293 5294 5336 5728 5730 5743 5973 6646 8807 8809 9173 929 952	Homo sapiens (human)
DOID:0060611	abdominal obesity-metabolic syndrome	LEP NEIL1 PPARGC1A	10891 3952 79661	Homo sapiens (human)

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