GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4626 - 4650** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
3990	lipase C, hepatic type	LIPC HL HTGL Triacylglycerol lipase	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 Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kuhnt-Junius degeneration Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation bacterial sepsis cancer cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis embryoma end stage renal disease endometriosis of uterus endometriosis essential hypertension familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis glucose intolerance glycogen storage disease II heart disease hepatitis hyperalphalipoproteinemia 1 hyperinsulinism hypertension hypothyroidism idiopathic scoliosis intermittent claudication ischemia kidney disease large intestine cancer lipid metabolism disorder lipoid nephrosis lung cancer lung non-small cell carcinoma macroglobulinemia macular degeneration marasmus myocardial infarction myxedema nephritis nephrosis nephrotic syndrome neurodegenerative disease nutmeg liver obesity obsolete lymphoplasmacytic lymphoma obsolete type 1 diabetes mellitus 9 peripheral artery disease peripheral vascular disease pre-eclampsia prediabetes syndrome protein-energy malnutrition pyoureter schizophrenia silent myocardial infarction 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 vascular disease
8513	lipase F, gastric type	LIPF HGL HLAL gastric triacylglycerol lipase	Wolman disease lipid storage disease lysosomal acid lipase deficiency stomach cancer stomach carcinoma
9388	lipase G, endothelial type	LIPG EDL	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 Duchenne muscular dystrophy Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myocardial infarction allergic asthma aortic atherosclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis autistic disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cholesterol-ester transfer protein deficiency coronary artery disease coronary thrombosis dementia depressive disorder diabetes mellitus diabetic cataract diabetic retinopathy embryoma embryonal cancer endometriosis of uterus endometriosis essential hypertension familial hypercholesterolemia familial retinoblastoma germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes heart disease hemolytic-uremic syndrome hyperalphalipoproteinemia 1 hypertension intrinsic asthma muscular dystrophy myocardial infarction nutmeg liver obesity ocular cancer placental insufficiency retinoblastoma sickle cell anemia silent myocardial infarction trilateral retinoblastoma type 2 diabetes mellitus uveal melanoma vascular disease
200879	lipase H	LIPH LPDLR PLA1B mPA-PLA1 mPA-PLA1alpha phospholipase A(1)
149998	lipase I	LIPI CT17 LPDL PLA1C PRED5 cancer/testis antigen 17 mPA-PLA1beta membrane-associated phospholipase A1 beta
142910	lipase family member J	LIPJ bA425M17.2
643414	lipase family member K	LIPK bA186O14.2
340654	lipase family member M	LIPM bA304I5.1
643418	lipase family member N	LIPN bA186O14.3
9516	lipopolysaccharide induced TNF factor	LITAF
3996	LLGL scribble cell polarity complex component 1	LLGL1
3993	LLGL scribble cell polarity complex component 2	LLGL2
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
10960	lectin, mannose binding 2	LMAN2 GP36B VIP36	neuroblastoma stomach cancer stomach carcinoma
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
55788	LMBR1 domain containing 1	LMBRD1
92255	LMBR1 domain containing 2	LMBRD2
64788	lipase maturation factor 1	LMF1
91289	lipase maturation factor 2	LMF2
4000	lamin A/C	LMNA
4001	lamin B1	LMNB1
84823	lamin B2	LMNB2
160492	lamin tail domain containing 1	LMNTD1
256329	lamin tail domain containing 2	LMNTD2

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