GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5701 - 5725** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
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
10637	left-right determination factor 1	LEFTY1
7044	left-right determination factor 2	LEFTY2
5641	legumain	LGMN
25802	leiomodin 1	LMOD1
442721	leiomodin 2	LMOD2
3982	lens intrinsic membrane protein 2	LIM2
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
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
9836	leucine carboxyl methyltransferase 2	LCMT2
116844	leucine rich alpha-2-glycoprotein 1	LRG1
100507055	leucine rich colipase like 1	LRCOL1
9211	leucine rich glioma inactivated 1	LGI1
10128	leucine rich pentatricopeptide repeat containing	LRPPRC
55203	leucine rich repeat LGI family member 2	LGI2
203190	leucine rich repeat LGI family member 3	LGI3
163175	leucine rich repeat LGI family member 4	LGI4
84894	leucine rich repeat and Ig domain containing 1	LINGO1
158038	leucine rich repeat and Ig domain containing 2	LINGO2
645191	leucine rich repeat and Ig domain containing 3	LINGO3
339398	leucine rich repeat and Ig domain containing 4	LINGO4
85444	leucine rich repeat and coiled-coil centrosomal protein 1	LRRCC1
57622	leucine rich repeat and fibronectin type III domain containing 1	LRFN1
57497	leucine rich repeat and fibronectin type III domain containing 2	LRFN2

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