GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5676 - 5700** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
3908	laminin subunit alpha 2	LAMA2
3909	laminin subunit alpha 3	LAMA3
3910	laminin subunit alpha 4	LAMA4
3911	laminin subunit alpha 5	LAMA5
3912	laminin subunit beta 1	LAMB1
3913	laminin subunit beta 2	LAMB2
3914	laminin subunit beta 3	LAMB3
22798	laminin subunit beta 4	LAMB4
3915	laminin subunit gamma 1	LAMC1
3918	laminin subunit gamma 2	LAMC2
10319	laminin subunit gamma 3	LAMC3
4047	lanosterol synthase	LSS OSC Oxidosqualene-lanosterol cyclase	Baraitser-Winter syndrome Fabry disease Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Q fever Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome Wolman disease acquired immunodeficiency syndrome acute lymphoblastic leukemia adult acute lymphocytic leukemia alopecia-mental retardation syndrome 4 alopecia ankylosing spondylitis arteriosclerotic cardiovascular disease atherosclerosis blindness bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract central nervous system cancer childhood acute lymphocytic leukemia childhood osteosarcoma chylomicron retention disease coronary artery disease diffuse idiopathic skeletal hyperostosis embryoma endometrial serous adenocarcinoma epilepsy epithelioid sarcoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma high grade glioma holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hypertension hypotrichosis 14 hypotrichosis 1 hypotrichosis intellectual disability learning disability lipid storage disease microcephaly mixed glioma orofaciodigital syndrome I orofaciodigital syndrome X ossification of the posterior longitudinal ligament of spine osteosarcoma ovary serous adenocarcinoma primary sclerosing cholangitis sarcoma sclerosing cholangitis senile cataract skin disease spinal stenosis spindle cell sarcoma squamous cell carcinoma tongue cancer tongue squamous cell carcinoma trypanosomiasis typhus visual epilepsy
55341	large 60S subunit nuclear export GTPase 1	LSG1 FLJ11301
9113	large tumor suppressor kinase 1	LATS1
26524	large tumor suppressor kinase 2	LATS2
448835	late cornified envelope 6A	LCE6A
4052	latent transforming growth factor beta binding protein 1	LTBP1
4053	latent transforming growth factor beta binding protein 2	LTBP2
4054	latent transforming growth factor beta binding protein 3	LTBP3
8425	latent transforming growth factor beta binding protein 4	LTBP4
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
150082	lebercilin LCA5 like	LCA5L
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
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
79748	lectin, mannose binding 1 like	LMAN1L ERGIC-53L ERGL

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