NR2E3

GENERAL INFORMATION

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Gene name

NR2E3

Gene description

Nuclear receptor subfamily 2, group E, member 3

Protein class

Disease related genes
Nuclear receptors
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Not detected

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Not detected

Organ

Expression



GENE INFORMATION

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Gene name

NR2E3 (HGNC Symbol)

Synonyms

PNR, rd7, RP37

Description

Nuclear receptor subfamily 2, group E, member 3 (HGNC Symbol)

Entrez gene summary

This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Chromosome

15

Cytoband

q23

Chromosome location (bp)

71792638 - 71818259

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000278570 (version 78.38)

Entrez gene

10002

UniProt

Q9Y5X4 (UniProt - Evidence at protein level)

neXtProt

NX_Q9Y5X4

Antibodypedia

NR2E3 antibodies


PROTEIN BROWSER

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ENST00000617575
 
ENST00000621098
 
ENST00000621736
 
 
 
 


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)

NR2E3-001 ENSP00000482504
ENST00000617575
Q9Y5X4
Show all »
Show » Show » 410 44.7 No 0
NR2E3-002 ENSP00000479962
ENST00000621098
Q9Y5X4
Show all »
Show » Show » 367 39.6 No 0
NR2E3-004 ENSP00000479254
ENST00000621736
Q8IVZ9
Show all »
Show » Show » 322 35.5 No 0