GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **5301 - 5325** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
987	LPS responsive beige-like anchor protein	LRBA
4026	LIM domain containing preferred translocation partner in lipoma	LPP
4025	lactoperoxidase	LPO
4023	lipoprotein lipase	LPL	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Crohn's colitis Crohn's disease Fabry disease Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Gilbert syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Norum disease Pick's disease Reye syndrome Richter's syndrome Tangier disease Wolman disease X-linked dilated cardiomyopathy Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acne acromegaly acute chest syndrome acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma age related macular degeneration alcoholic pancreatitis aortic atherosclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive hypercholesterolemia bilirubin metabolic disorder bone osteosarcoma brain infarction brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease carotid artery thrombosis carotid stenosis celiac disease central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma cholesterol-ester transfer protein deficiency choreaacanthocytosis chronic kidney disease chronic lymphocytic leukemia chylomicron retention disease colon cancer colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma cystic lymphangioma cystinuria degeneration of macula and posterior pole dementia diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism eclampsia embryoma embryonal cancer end stage renal disease endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy essential hypertension extramedullary plasmacytoma familial apolipoprotein A5 deficiency familial apolipoprotein C-II deficiency familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial lipase maturation factor 1 deficiency familial lipoprotein lipase deficiency familial partial lipodystrophy type 2 familial partial lipodystrophy focal segmental glomerulosclerosis follicular lymphoma galactosemia germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes gliosarcoma glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hematologic cancer hepatitis C hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hyperinsulinism hyperlipoproteinemia type III hyperlipoproteinemia type IV hyperlipoproteinemia type V hyperpituitarism hyperprolactinemia hypertension hypertrophic cardiomyopathy hypoglycemia hypolipoproteinemia impotence inflammatory bowel disease 1 inflammatory bowel disease isolated growth hormone deficiency large intestine cancer lipid storage disease lipoatrophic diabetes mellitus lipodystrophy liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia macular degeneration maple syrup urine disease mastitis metabolic dysfunction-associated steatotic liver disease mixed glioma monoclonal gammopathy of uncertain significance morbid obesity multiple myeloma multiple sclerosis muscular disease myocardial infarction myotonic dystrophy type 1 myotonic dystrophy type 2 neurodegenerative disease nodular prostate nutmeg liver obesity obsolete familial hypertriglyceridemia obsolete lymphoplasmacytic lymphoma obsolete type 1 diabetes mellitus 9 osteosarcoma ovarian hyperstimulation syndrome overnutrition pancreatitis peripheral artery disease placental insufficiency plasma cell neoplasm plasmacytoma polycystic ovary syndrome polycythemia vera pre-eclampsia prediabetes syndrome premature ejaculation prostate cancer prostate carcinoma prostatic adenoma psychologic dyspareunia sarcomatoid carcinoma schizophrenia silent myocardial infarction steatotic liver disease thrombophilia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis uterine corpus cancer vascular disease visceral leishmaniasis
64900	lipin 3	LPIN3 SMP2	lipid metabolism disorder lung cancer lung non-small cell carcinoma myoglobinuria obesity
9663	lipin 2	LPIN2 KIAA0249	Chanarin-Dorfman syndrome Crohn's colitis Crohn's disease Diamond-Blackfan anemia SAPHO syndrome acne agranulocytosis allergic asthma anemia asthma autosomal recessive congenital ichthyosis 1 autosomal recessive osteopetrosis 7 cancer chronic recurrent multifocal osteomyelitis congenital dyserythropoietic anemia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypoplastic anemia congestive heart failure dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism familial mediterranean fever familial periodic paralysis fibromyalgia gastrointestinal system disease glomerulonephritis granular corneal dystrophy 2 ichthyosis inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrinsic asthma keratosis follicularis leukopenia lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy macrocytic anemia mevalonic aciduria microcytic anemia mongolian spot myoglobinuria myopathy myopia myositis nephritis neutropenia obesity obsolete congenital ichthyosiform erythroderma osteomyelitis osteopetrosis osteosclerosis prostate cancer prostate carcinoma proteinuria pseudoxanthoma elasticum relapsing fever rheumatoid arthritis severe congenital neutropenia synovitis tenosynovitis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue type 2 diabetes mellitus ulcerative colitis
23175	lipin 1	LPIN1 KIAA0188 phosphatidate phosphatase LPIN1	46,XY sex reversal Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Pearson syndrome Richter's syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute kidney failure adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cervix uteri carcinoma in situ chronic kidney disease chronic lymphocytic leukemia colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 diabetes mellitus diabetic ketoacidosis embryoma end stage renal disease essential hypertension familial periodic paralysis fibromyalgia gastroenteritis gestational diabetes glucose intolerance heart disease hepatoblastoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hyperinsulinism hypertension ileitis ileocolitis isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma middle cerebral artery infarction morbid obesity motor peripheral neuropathy myoglobinuria myopathy myositis neuropathy obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polycystic ovary syndrome polyneuropathy prediabetes syndrome prostate cancer prostate carcinoma retinitis pigmentosa 9 sarcomatoid carcinoma steatotic liver disease type 2 diabetes mellitus very long chain acyl-CoA dehydrogenase deficiency
9926	lysophosphatidylglycerol acyltransferase 1	LPGAT1 FAM34A1 KIAA0205 LPLAT7 NET8 lysophospholipid acyltransferase 7	depressive disorder major depressive disorder melancholic depression neurotic disorder obesity obsolete melancholia
254531	lysophosphatidylcholine acyltransferase 4	LPCAT4 FLJ10257 LPAAT-eta LPEAT2 LPLAT10 lysophosphatidylethanolamine acyltransferase 2 lysophospholipid acyltransferase 10	colorectal cancer colorectal carcinoma large intestine cancer
10162	lysophosphatidylcholine acyltransferase 3	LPCAT3 C3F LPLAT12 Lysophospholipid acyltransferase 5 lysophospholipid acyltransferase 12 nessy	allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis beta thalassemia cancer coronary artery disease essential hypertension hepatocellular carcinoma hyperglycemia hypertension intrinsic asthma liver cancer nutmeg liver sickle cell anemia thalassemia vascular disease
54947	lysophosphatidylcholine acyltransferase 2	LPCAT2 AGPAT11 FLJ20481 LPLAT9 LysoPAFAT lysophospholipid acyltransferase 9	colorectal cancer colorectal carcinoma large intestine cancer microphthalmia obsolete Matthew-Wood syndrome polycystic ovary syndrome prostate cancer prostate carcinoma
79888	lysophosphatidylcholine acyltransferase 1	LPCAT1 AGPAT10 AGPAT9 FLJ12443 LPLAT8 lysophospholipid acyltransferase 8	Leber congenital amaurosis adult respiratory distress syndrome allergic asthma asthma breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy cystic fibrosis embryoma fundus albipunctatus hepatitis C hepatocellular carcinoma hypereosinophilic syndrome intrinsic asthma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microglandular adenosis newborn respiratory distress syndrome nonpapillary renal cell carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa sarcomatoid renal cell carcinoma sickle cell anemia
10161	lysophosphatidic acid receptor 6	LPAR6
57121	lysophosphatidic acid receptor 5	LPAR5
2846	lysophosphatidic acid receptor 4	LPAR4
23566	lysophosphatidic acid receptor 3	LPAR3
1902	lysophosphatidic acid receptor 1	LPAR1
4018	lipoprotein(a)	LPA
84171	lysyl oxidase like 4	LOXL4
84695	lysyl oxidase like 3	LOXL3
4017	lysyl oxidase like 2	LOXL2
4016	lysyl oxidase like 1	LOXL1
125336	lipoxygenase homology PLAT domains 1	LOXHD1
4015	lysyl oxidase	LOX
91694	LON peptidase N-terminal domain and ring finger 1	LONRF1

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