RFX6

GENERAL INFORMATION

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Gene name

RFX6

Gene description

Regulatory factor X, 6

Protein class

Disease related genes
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (adrenal gland, stomach)
GTEx:Tissue enhanced (pancreas, stomach)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in islets of Langerhans, stomach and large intestine.

ANTIBODY RELIABILITY

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Data reliability
description

Presumed off target binding observed and disregarded. External characterization data supports antibody staining.

Data reliability

Uncertain based on 1 antibody.
HPA037696
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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

Pancreas

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 enhanced (adrenal gland, stomach)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (pancreas, stomach)

Organ

Expression



GENE INFORMATION

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Gene name

RFX6 (HGNC Symbol)

Synonyms

dJ955L16.1, MGC33442, RFXDC1

Description

Regulatory factor X, 6 (HGNC Symbol)

Entrez gene summary

The nuclear protein encoded by this gene is a member of the regulatory factor X (RFX) family of transcription factors. Studies in mice suggest that this gene is specifically required for the differentiation of islet cells for the production of insulin, but not for the differentiation of pancreatic polypeptide-producing cells. It regulates the transcription factors involved in beta-cell maturation and function, thus, restricting the expression of the beta-cell differentiation and specification genes. Mutations in this gene are associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis.[provided by RefSeq, Sep 2010]

Chromosome

6

Cytoband

q22.1

Chromosome location (bp)

116877212 - 116932163

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000185002 (version 78.38)

Entrez gene

222546

UniProt

Q8HWS3 (UniProt - Evidence at protein level)

neXtProt

NX_Q8HWS3

Antibodypedia

RFX6 antibodies


PROTEIN BROWSER

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ENST00000332958
 
 
 
 


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)

RFX6-001 ENSP00000332208
ENST00000332958
Q8HWS3
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