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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 **2201 - 2225** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:3320	Tay-Sachs disease Aliases: GM2 gangliosidosis, type 1 hexosaminidase A deficiency	Hexa	300757	Rattus norvegicus (Norway rat)
DOID:10211	cholelithiasis	Ugt1a1	394436	Mus musculus (house mouse)
DOID:8893	psoriasis	gba-3 gba-4	177314 178535	Caenorhabditis elegans
DOID:0111452	progressive myoclonus epilepsy 1A Aliases: EPM1A	ARSA ASAH1 EPM2A NEU1 PFKL PRNP TMED9	410 427 4758 5211 54732 5621 7957	Homo sapiens (human)
DOID:0050861	colorectal adenocarcinoma	GPX1 GPX2	852546 853842	Saccharomyces cerevisiae S288C
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	MGAT2	4247	Homo sapiens (human)
DOID:2838	stress polycythemia Aliases: Gaisbock's syndrome Polycythemia, emotional	ACO1 BPGM CD177 CYB5R3 FH FUT1 G6PD HPRT1 PKLR SMUG1	1727 2271 23583 2523 2539 3251 48 5313 57126 669	Homo sapiens (human)
DOID:4977	lymphedema Aliases: Lymphatic edema Lymphoedema	Pgf	18654	Mus musculus (house mouse)
DOID:1442	obsolete Alpers syndrome	PRNP	5621	Homo sapiens (human)
DOID:1073	renal hypertension	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:2043	hepatitis B Aliases: chronic hepatitis B hepatitis B infection	ATG26	850886	Saccharomyces cerevisiae S288C
DOID:8738	leukoplakia of penis Aliases: Kraurosis of penis Penile Leukoplakia	INPP5E	56623	Homo sapiens (human)
DOID:615	leukopenia Aliases: Leucopenia	ABO ADH1B AKR1B1 ALDH2 ATP6AP1 B3GAT1 CAT CD177 CD33 CEL CHPT1 CYP1A1 CYP1B1 CYP2B6 CYP2C19 CYP2C8 CYP2C9 CYP39A1 CYP3A4 CYP3A5 DCTD DHDDS EOGT FASN FCGR3B FH G6PC1 G6PC3 GBA1 HMGCL HMMR HPGDS HPRT1 ICAM1 IDUA LPIN2 MBL2 MMUT NAAA NCAM1 PARP1 PARP9 PIK3C2A PIK3CA PIK3CB PIK3CD PIK3CG PTGS2 SELE SELL SELP SFTPD SLC17A5 SLC27A5 SLC35A2 SLC37A4 SUCLA2 TMTC3 TNFRSF10C UGGT1 UGT1A10 UGT1A1 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9 UGT2B7 UMPS	1056 10998 125 142 1543 1545 1555 1557 1558 1559 1576 1577 160418 1635 217 2194 2215 2271 231 2538 2542 2629 26503 27087 27163 27306 28 285203 3155 3161 3251 3383 3425 4153 4594 4684 51302 5286 5290 5291 5293 5294 537 54575 54576 54577 54578 54579 54600 54657 54658 54659 56886 56994 57126 5743 6401 6402 6403 6441 7355 7364 7372 79947 83666 847 8794 8803 92579 945 9663	Homo sapiens (human)
DOID:1338	congenital dyserythropoietic anemia Aliases: congenital dyshaematopoietic anaemia	Man2a1	17158	Mus musculus (house mouse)
DOID:13544	low tension glaucoma Aliases: Normal tension glaucoma	Adrb1 Tlr4 Tnf Tp53	24835 24842 24925 29260	Rattus norvegicus (Norway rat)
DOID:13910	red color blindness Aliases: Protan defect Protanopia	ACO2 CA4 CACNA2D4 CD74 ELOVL4 G6PD HS6ST1 MBD4 NYX PCYT1A PKD1 SDHC STS	2539 412 50 5130 5310 60506 6391 6785 762 8930 93589 9394 972	Homo sapiens (human)
DOID:5160	arteriosclerosis obliterans	PIK3CA PIK3CB PIK3CD PIK3CG SOAT1	5290 5291 5293 5294 6646	Homo sapiens (human)
DOID:1574	alcohol use disorder Aliases: Ethanol abuse alcohol abuse	Akt1 Akt2 Atp1a2 Comt Gsto2 Htr2a Igf2 Ppp1r3b Ppp1r3c St6gal1	192280 24185 24212 24267 24483 25197 25233 29595 309465 309513	Rattus norvegicus (Norway rat)
DOID:635	acquired immunodeficiency syndrome Aliases: AIDS acquired Immune deficiency	Igf2 Tnf	24483 24835	Rattus norvegicus (Norway rat)
DOID:13317	hyperinsulinemic hypoglycemia Aliases: Islet cell hyperplasia nesidioblastosis persistent hyperinsulinemia hypoglycemia of infancy	Gck	103988	Mus musculus (house mouse)
DOID:0060551	poikiloderma with neutropenia Aliases: poikiloderma with neutropenia, Clericuzio type	ENOSF1 GPX1 GPX3 MAG PLCB1	23236 2876 2878 4099 55556	Homo sapiens (human)
DOID:0110858	polycystic kidney disease 1 Aliases: Apkd1 Pkd1 Polycystic Kidney Disease, Adult, Type I	ACE ALG9 APRT DCN GANAB HAGH KL LGALS3 PDHX PGD PGP PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKD2 PRKAA2 PRKCSH PTGS2 SEMA7A SMUG1 SOAT1 UMOD	1634 1636 23193 23583 283871 3029 353 3958 5226 5290 5291 5293 5294 5310 5311 5563 5589 5743 6646 7369 79796 8050 8482 9365	Homo sapiens (human)
DOID:0080322	polycystic kidney disease	algn-5 sqv-6	178822 190099	Caenorhabditis elegans
DOID:0080557	congenital disorder of glycosylation Ie Aliases: congenital disorder of glycosylation 1e	dpm1	445202	Danio rerio (zebrafish)
DOID:7210	psammomatous meningioma	ALDH1A3 ALOX5 ALPL CD33 CD44 CD55 CYP19A1 CYP1A1 CYP1B1 CYP4F3 DHCR24 ENO2 FASN FCGR3B FOLR1 GAPDH GPX1 HPGDS HPRT1 IL18R1 LARGE1 LGALS1 LGALS3 MMP25 MMUT MSLN MUTYH NT5E NTHL1 OGA PIK3CA PIK3CB PIK3CD PIK3CG PLA2G1B PLA2G2A PLA2G6 PLA2G7 PLAUR PLB1 PTEN PTGDS PTGS1 PTGS2 SDHB SDHC SDHD SMUG1 SOAT1 STS TIPARP TNKS VCAN	10232 10724 1462 151056 1543 1545 1588 1604 1718 2026 2194 220 2215 2348 23583 240 249 2597 25976 27306 2876 3251 3956 3958 4051 412 4594 4595 4907 4913 5290 5291 5293 5294 5319 5320 5329 5728 5730 5742 5743 6390 6391 6392 64386 6646 7941 8398 8658 8809 9215 945 960	Homo sapiens (human)

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