GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4276 - 4300** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
100507055	leucine rich colipase like 1	LRCOL1
116844	leucine rich alpha-2-glycoprotein 1	LRG1
9836	leucine carboxyl methyltransferase 2	LCMT2
3953	leptin receptor	LEPR	arteriosclerosis chronic kidney disease chronic obstructive pulmonary disease congestive heart failure coronary artery disease diastolic heart failure dilated cardiomyopathy glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypertension metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoporosis pancreatitis pre-eclampsia primary biliary cholangitis proteinuria renal fibrosis short bowel syndrome sleep apnea type 2 diabetes mellitus
3952	leptin	LEP	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acute pancreatitis adult respiratory distress syndrome alcohol dependence alcoholic liver cirrhosis asthma breast cancer chronic obstructive pulmonary disease congenital leptin deficiency cystic fibrosis end stage renal disease familial hyperlipidemia gestational diabetes glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma hyperinsulinism hypertension hypogonadism lipid metabolism disorder lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoarthritis osteoporosis pre-eclampsia primary biliary cholangitis renal cell carcinoma rhinitis short bowel syndrome steatotic liver disease type 2 diabetes mellitus
3982	lens intrinsic membrane protein 2	LIM2
442721	leiomodin 2	LMOD2
25802	leiomodin 1	LMOD1
5641	legumain	LGMN
7044	left-right determination factor 2	LEFTY2
10637	left-right determination factor 1	LEFTY1
81562	lectin, mannose binding 2 like	LMAN2L DKFZp564L2423 VIP36-like VIPL	agnosia attention deficit hyperactivity disorder autosomal dominant intellectual developmental disorder autosomal recessive intellectual developmental disorder 52 bipolar disorder borderline personality disorder cerebral degeneration choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy intermittent explosive disorder lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary adenocarcinoma papillary renal cell carcinoma partial motor epilepsy pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 thyroid gland papillary carcinoma visual epilepsy
10960	lectin, mannose binding 2	LMAN2 GP36B VIP36	neuroblastoma stomach cancer stomach carcinoma
79748	lectin, mannose binding 1 like	LMAN1L ERGIC-53L ERGL
3998	lectin, mannose binding 1	LMAN1 ERGIC-53 ERGIC53 FMFD1 MCFD1 MR60 endoplasmic reticulum-golgi intermediate compartment protein 53 gp58	IgA glomerulonephritis adenocarcinoma adenoma allergic disease arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer carcinoma colorectal cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease factor V deficiency factor VII deficiency factor VIII deficiency factor XIII deficiency follicular adenoma hematopoietic system disease large intestine cancer malaria microcystic adenoma nutmeg liver obsolete inherited blood coagulation disease papillary adenoma sarcomatoid carcinoma thanatophoric dysplasia vitamin K deficiency bleeding
3931	lecithin-cholesterol acyltransferase	LCAT phosphatidylcholine--sterol O-acyltransferase	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 Bloom syndrome 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 2 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 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 Norum disease Pick's disease Reye syndrome Tangier disease abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acute chest syndrome acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anemia aortic atherosclerosis arcus senilis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness brain stem infarction cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency choreaacanthocytosis chronic kidney disease chylomicron retention disease congestive heart failure corneal dystrophy coronary artery disease coronary thrombosis disease of metabolism dry eye syndrome end stage renal disease familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial lipoprotein lipase deficiency familial nephrotic syndrome gallbladder disease glomerulonephritis granular corneal dystrophy heart disease hemolytic anemia hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hyperalphalipoproteinemia 1 hyperlipoproteinemia type V hypolipoproteinemia inherited metabolic disorder kidney disease kidney failure lipoid nephrosis liver cancer liver disease macrocytic anemia macular corneal dystrophy motor peripheral neuropathy myocardial infarction nephritis nephrosis nephrotic syndrome nutmeg liver obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum ovarian cancer ovarian carcinoma proteinuria pyoureter recurrent corneal erosion renal osteodystrophy rheumatoid arthritis sickle cell anemia silent myocardial infarction steatotic liver disease uremia xerophthalmia
150082	lebercilin LCA5 like	LCA5L
143903	layilin	LAYN FLJ30977 FLJ31092	arthritis arthropathy bronchus cancer bronchus carcinoma cancer chronic obstructive pulmonary disease colitis colon cancer colonic benign neoplasm colorectal cancer embryoma gastroenteritis gliosarcoma glomerulonephritis high grade glioma ileitis ileocolitis kidney disease large intestine cancer lung cancer lung carcinoma mixed glioma nephritis osteoarthritis
8425	latent transforming growth factor beta binding protein 4	LTBP4
4054	latent transforming growth factor beta binding protein 3	LTBP3
4053	latent transforming growth factor beta binding protein 2	LTBP2
4052	latent transforming growth factor beta binding protein 1	LTBP1
448835	late cornified envelope 6A	LCE6A
26524	large tumor suppressor kinase 2	LATS2
9113	large tumor suppressor kinase 1	LATS1

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