GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **14826 - 14850** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:1205	allergic disease Aliases: allergic hypersensitivity disease hypersensitivity hypersensitivity reaction type I disease	ACE AGT AKR1B1 CD14 CYSLTR1 FCGR3A HLA-DQA1 HLA-DQB1 HLA-DRA HLA-DRB1 ICAM1 IL13 LTA MIF TAP1	10800 1636 183 2214 231 3117 3119 3122 3123 3383 3596 4049 4282 6890 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050848	obstructive sleep apnea Aliases: obstructive sleep apnea syndrome	ABCB1 ACE ADORA1 ADRB1 BDNF BMP7 CCL2 CCL5 CYSLTR1 CYSLTR2 EDN1 EDNRA GHRL GHSR HP ICAM1 IL10 IL6 LEP LEPR MMP9 MUC1 NGF NOS2 NOS3 NR3C1 NRG1 NTRK1 PLA2G7 PTGS2 RELA SERPINE1 SFTPB SLC6A4 TNF TNFRSF1A	10800 134 153 1636 1906 1909 2693 2908 3084 3240 3383 3569 3586 3952 3953 4318 4582 4803 4843 4846 4914 5054 51738 5243 57105 5743 5970 627 6347 6352 6439 6532 655 7124 7132 7941	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111862	congenital bilateral absence of vas deferens Aliases: CAVD CBAVD congenital bilateral agenesis of vas deferens congenital bilateral aplasia of vas deferens	CFTR	1080	Homo sapiens (human)	Alliance of Genome Resources
DOID:5733	salpingitis	CFTR	1080	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111864	autosomal recessive congenital bilateral absence of vas deferens	CFTR	1080	Homo sapiens (human)	Alliance of Genome Resources
DOID:13316	exocrine pancreatic insufficiency Aliases: EPI	CFTR	1080	Homo sapiens (human)	Alliance of Genome Resources
DOID:693	dental enamel hypoplasia Aliases: enamel hypoplasia	CFTR	1080	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080526	bronchiectasis 1	CFTR SCNN1B	1080 6338	Homo sapiens (human)	Alliance of Genome Resources
DOID:4988	alcoholic pancreatitis	CCK CFTR UGT1A7	1080 54577 885	Homo sapiens (human)	Alliance of Genome Resources
DOID:1724	duodenal ulcer Aliases: Curling Ulcer Curling's ulcers Stress Ulcer	ACO1 CFTR SLC11A2 STAT3 TFRC VEGFA	1080 48 4891 6774 7037 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:9563	bronchiectasis Aliases: Polynesian bronchiectasis	CFTR MBL2 MMP9 TAP1 TNF	1080 4153 4318 6890 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:13166	allergic bronchopulmonary aspergillosis Aliases: pulmonary aspergillus disease	CFTR HLA-DQB1 HLA-DRB1 MBL2 TLR9 TNFRSF1A	1080 3119 3123 4153 54106 7132	Homo sapiens (human)	Alliance of Genome Resources
DOID:13258	typhoid fever Aliases: Typhoid	CFTR HLA-DQB1 HLA-DRB1 LTA TNF	1080 3119 3123 4049 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050127	sinusitis	CFB CFTR CHIA IL13 IL2 LTA MMP9 MUC5B NR3C1 PDGFB PLAU PLAUR SFTPA1 SFTPD TLR2 TLR4 TLR9	1080 27159 2908 3558 3596 4049 4318 5155 5328 5329 54106 629 6441 653509 7097 7099 727897	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060643	primary sclerosing cholangitis	ABCB4 CFTR DNASE1 GNRHR HLA-DQB1 KRT18 TNF VEGFA	1080 1773 2798 3119 3875 5244 7124 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:10211	cholelithiasis	APOE CCKAR CFTR CYP17A1 UGT1A1	1080 1586 348 54658 886	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110861	autosomal recessive polycystic kidney disease Aliases: Arpkd Pkhd1 Polycystic Kidney Disease, Infantile, Type I Polycystic Kidney and Hepatic Disease 1	ACE AKT1 AQP1 ARL3 BICC1 C3 CD14 CDC25A CFTR CYP4A11 CYP4A22 ELN GPBAR1 MTOR NEK1 PANX1 PIK3CA PKD1 PKHD1 SLC4A2 TMEM67 TSC1	1080 151306 1579 1636 2006 207 24145 2475 284541 358 403 4750 5290 5310 5314 6522 718 7248 80114 91147 929 993	Homo sapiens (human)	Alliance of Genome Resources
DOID:11132	prostatic hypertrophy	AR BAD CASP6 CFTR CLU ESR1 FADD FGF7 FGF8 IGF1R IL13 IL3 IL5 KDR MYC NME2 PDGFB PDGFD PTGS2 RELA SRD5A1	1080 1191 2099 2252 2253 3480 3562 3567 3596 367 3791 4609 4831 5155 572 5743 5970 6715 80310 839 8772	Homo sapiens (human)	Alliance of Genome Resources
DOID:10808	gastric ulcer Aliases: acute gastric ulcer with haemorrhage and perforation acute gastric ulcer with hemorrhage AND with perforation but without obstruction acute gastric ulcer with hemorrhage and obstruction acute gastric ulcer with hemorrhage and perforation acute gastric ulcer with hemorrhage and perforation, with obstruction acute gastric ulcer with hemorrhage and perforation, without mention of obstruction acute gastric ulcer with hemorrhage, with obstruction acute gastric ulcer with hemorrhage, with perforation AND with obstruction acute gastric ulcer with perforation acute gastric ulcer with perforation AND obstruction acute gastric ulcer with perforation, with obstruction acute gastric ulcer without hemorrhage and without perforation acute gastric ulcer without hemorrhage, without perforation AND without obstruction acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction bleeding acute gastric ulcer chronic gastric ulcer without hemorrhage AND without perforation chronic gastric ulcer without hemorrhage AND without perforation but with obstruction chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction	AGT ANGPT1 ANGPT2 BAD CAT CBLIF CFTR COL18A1 F13A1 FAS FASLG FOS FOXO4 HRH3 IDUA IL25 MMP13 MMP2 MMP3 MMP9 MUC5AC MUC6 NOS3 OXTR PTGER1 PTGS2 TEK TFF1 TIMP1	1080 11255 183 2162 2353 2694 284 285 3425 355 356 4303 4313 4314 4318 4322 4586 4588 4846 5021 572 5731 5743 64806 7010 7031 7076 80781 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:13406	pulmonary sarcoidosis Aliases: lung Sarcoidosis	ABO BDNF C3 CCL5 CCR5 CCR7 CFTR CHI3L1 CXCR3 DEFB1 EGR1 HLA-DRB1 IL15 IL18R1 IL1RN LTA MUC1 NGF NOD2 NOS2 NR3C1 NTF3 NTRK1 SFTPA1 TGFB1 TLR2 TNC TNF TNFRSF1B	1080 1116 1234 1236 1672 1958 28 2833 2908 3123 3371 3557 3600 4049 4582 4803 4843 4908 4914 627 6352 64127 653509 7040 7097 7124 7133 718 8809	Homo sapiens (human)	Alliance of Genome Resources
DOID:1682	congenital heart disease Aliases: Congenital Heart Defects Congenital anomaly of heart Heart Malformation congenital heart defect heart defect	ADAMTS19 ADCY2 CDC34 CHD6 CHD7 CHD8 CHD9 CMA1 CRIPTO DNMT1 FOXP1 GATA4 GDF1 GPX3 HCFC1 HCFC2 ITPR1 JAG1 JPT1 KMT2A KMT2B KMT2C KMT2D LEFTY2 LRP2 MYBPC1 MYBPC2 MYBPC3 MYH7 NAA15 NAA16 NFATC1 NOTCH1 PLCB2 RFC1 RNF20 RNF40 RPS24 SAP130 SMYD4 SON SP4 TAB2 TLL1 UBE2R2 USP17L3 USP42 VEGFA WDR5	108 11091 114826 1215 171019 1786 182 23118 2626 2657 27086 2878 29915 3054 3708 4036 4297 4604 4606 4607 4625 4772 4851 51155 5330 54926 55636 56254 57680 58508 5981 6229 645836 6651 6671 6997 7044 7092 7422 79595 79612 80155 80205 8085 84132 84181 9757 9810 997	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070047	Schuurs-Hoeijmakers Syndrome Aliases: MRD17 SHMS autosomal dominant mental retardation 17	Pacs1	107975	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070529	Sifrim-Hitz-Weiss syndrome Aliases: CHD4 Neurodevelopmental Disorder CHD4-related neurodevelopmental disorder CHD4-related neurodevelopmental syndrome SIFRIM-HITZ-WEISS MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION SYNDROME SIHIWES	Chd4	107932	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060480	left ventricular noncompaction Aliases: left ventricular hypertrabeculation	Chd4 Slc39a8 Ywhae	107932 22627 67547	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060058	lymphoma Aliases: lymphoid cancer	Chd4 Rela	107932 19697	Mus musculus (house mouse)	Alliance of Genome Resources

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