RRBP1

GENERAL INFORMATION

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Gene name

RRBP1

Gene description

Ribosome binding protein 1

Protein class

Plasma proteins
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

8
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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 expression in all tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA009026 , HPA011924
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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

Fallopian tube



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

RRBP1 (HGNC Symbol)

Synonyms

ES/130, hES

Description

Ribosome binding protein 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12. [provided by RefSeq, Apr 2012]

Chromosome

20

Cytoband

p12.1

Chromosome location (bp)

17613678 - 17682295

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000125844 (version 78.38)

Entrez gene

6238

UniProt

Q9P2E9 (UniProt - Evidence at protein level)

neXtProt

NX_Q9P2E9

Antibodypedia

RRBP1 antibodies


PROTEIN BROWSER

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ENST00000246043
 
ENST00000360807
 
ENST00000377807
 
ENST00000377813
 
ENST00000398782
 
ENST00000455029
 
ENST00000470422
 
ENST00000610403
 
 
 
 


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)

RRBP1-001 ENSP00000354045
ENST00000360807
Q9P2E9
Show all »
Show » Show » 977 108.6 No 1
RRBP1-002 ENSP00000367044
ENST00000377813
F8W7S5
Show all »
Show » Show » 1410 152.5 No 1
RRBP1-003 ENSP00000381762
ENST00000398782
A2A2S5
Show all »
Show » Show » 300 31.7 No 0
RRBP1-005 ENSP00000478324
ENST00000470422
Show » 346 38.7 No 0
RRBP1-007 ENSP00000401206
ENST00000455029
F8W7S5
Show all »
Show » Show » 751 84.3 No 0
RRBP1-201 ENSP00000246043
ENST00000246043
F8W7S5
Show all »
Show » Show » 1410 152.5 No 1
RRBP1-202 ENSP00000367038
ENST00000377807
Q9P2E9
Show all »
Show » Show » 977 108.6 No 1
RRBP1-203 ENSP00000479709
ENST00000610403
F8W7S5
Show all »
Show » Show » 934 102.8 No 0