IDE

GENERAL INFORMATION

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Gene name

IDE

Gene description

Insulin-degrading enzyme

Protein class

Enzymes
FDA approved drug targets
Plasma proteins
Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Normal tissues showed weak to moderate cytoplasmic and/or membranous positivity. Stomach, small intestine and muscles exhibited strong positivity. Glial cells, soft tissues and endometrial stromal cells were negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA063478
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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

Stomach

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

IDE

Synonyms

Description

Insulin-degrading enzyme (HGNC Symbol)

Entrez gene summary

This gene encodes a zinc metallopeptidase that degrades intracellular insulin, and thereby terminates insulins activity, as well as participating in intercellular peptide signalling by degrading diverse peptides such as glucagon, amylin, bradykinin, and kallidin. The preferential affinity of this enzyme for insulin results in insulin-mediated inhibition of the degradation of other peptides such as beta-amyloid. Deficiencies in this protein's function are associated with Alzheimer's disease and type 2 diabetes mellitus but mutations in this gene have not been shown to be causitive for these diseases. This protein localizes primarily to the cytoplasm but in some cell types localizes to the extracellular space, cell membrane, peroxisome, and mitochondrion. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described but have not been experimentally verified.[provided by RefSeq, Sep 2009]

Chromosome

10

Cytoband

q23.33

Chromosome location (bp)

92451684 - 92574076

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000119912 (version 78.38)

Entrez gene

3416

UniProt

P14735 (UniProt - Evidence at protein level)

neXtProt

NX_P14735

Antibodypedia

IDE antibodies


PROTEIN BROWSER

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ENST00000265986
 
ENST00000371581
 
ENST00000436178
 
 
 
 


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)

IDE-001 ENSP00000265986
ENST00000265986
P14735
Show all »
Show » Show » 1019 118 Yes 0
IDE-007 ENSP00000408850
ENST00000436178
Q5T5N3
Show all »
Show » Show » 257 29.2 No 0
IDE-201 ENSP00000360637
ENST00000371581
P14735
Show all »
Show » Show » 464 54.2 No 0