UTRN

GENERAL INFORMATION

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Gene name

UTRN

Gene description

Utrophin

Protein class

Cytoskeleton related proteins
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

9
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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

Cytoplasmic an membranous expression in most tissues with highest levels in endothelium, stomach, pancreas, prostate and respiratory epithelium.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA018894 , CAB016348
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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

Colon

Kidney

Testis

Prostate



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

UTRN (HGNC Symbol)

Synonyms

DMDL, DRP, DRP1

Description

Utrophin (HGNC Symbol)

Entrez gene summary

This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008]

Chromosome

6

Cytoband

q24.2

Chromosome location (bp)

144285701 - 144853034

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000152818 (version 78.38)

Entrez gene

7402

UniProt

P46939 (UniProt - Evidence at protein level)

neXtProt

NX_P46939

Antibodypedia

UTRN antibodies


PROTEIN BROWSER

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ENST00000367524
 
ENST00000367525
 
ENST00000367526
 
ENST00000367545
 
ENST00000417142
 
ENST00000421035
 
ENST00000432686
 
ENST00000433557
 
ENST00000455022
 
 
 
 


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)

UTRN-001 ENSP00000356515
ENST00000367545
P46939
Show all »
Show » Show » 3433 394.5 No 0
UTRN-002 ENSP00000396276
ENST00000421035
Show » Show » 154 17.4 No 0
UTRN-003 ENSP00000390879
ENST00000433557
Q5SYY2
Show all »
Show » 47 5.5 No 0
UTRN-004 ENSP00000398923
ENST00000432686
Q5JT45
Show all »
Show » Show » 181 20.8 No 0
UTRN-005 ENSP00000404205
ENST00000417142
Q5JT44
Show all »
Show » Show » 184 21 No 0
UTRN-006 ENSP00000387927
ENST00000455022
Q5JT49
Show all »
Show » Show » 186 21.4 No 0
UTRN-007 ENSP00000356494
ENST00000367524
Show » Show » 251 28.5 No 0
UTRN-008 ENSP00000356495
ENST00000367525
Q5T098
Show all »
Show » 66 7.8 No 0
UTRN-010 ENSP00000356496
ENST00000367526
Q5T097
Show all »
Show » Show » 988 113.4 No 0