LEP

GENERAL INFORMATION

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Gene name

LEP

Gene description

Leptin

Protein class

Cancer-related genes
Candidate cardiovascular disease genes
Disease related genes
Plasma proteins
Predicted secreted proteins

Predicted localization

Secreted

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (adipose tissue)
GTEx:Group enriched (adipose tissue, breast)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in selected tissues with positivity in plasma.

ANTIBODY RELIABILITY

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Data reliability
description

Secreted protein, tissue location of RNA and protein might differ and correlation is complex. Pending retesting.

Data reliability

Uncertain based on 3 antibodies.
HPA030721 , CAB010490 , CAB016730
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Duodenum

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (adipose tissue)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (adipose tissue, breast)

Organ

Expression



GENE INFORMATION

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Gene name

LEP (HGNC Symbol)

Synonyms

OB, OBS

Description

Leptin (HGNC Symbol)

Entrez gene summary

This gene encodes a protein that is secreted by white adipocytes, and which plays a major role in the regulation of body weight. This protein, which acts through the leptin receptor, functions as part of a signaling pathway that can inhibit food intake and/or regulate energy expenditure to maintain constancy of the adipose mass. This protein also has several endocrine functions, and is involved in the regulation of immune and inflammatory responses, hematopoiesis, angiogenesis and wound healing. Mutations in this gene and/or its regulatory regions cause severe obesity, and morbid obesity with hypogonadism. This gene has also been linked to type 2 diabetes mellitus development. [provided by RefSeq, Jul 2008]

Chromosome

7

Cytoband

q32.1

Chromosome location (bp)

128241284 - 128257628

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000174697 (version 78.38)

Entrez gene

3952

UniProt

P41159 (UniProt - Evidence at protein level)

neXtProt

NX_P41159

Antibodypedia

LEP antibodies


PROTEIN BROWSER

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ENST00000308868
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

LEP-001 ENSP00000312652
ENST00000308868
P41159
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