RNF213

GENERAL INFORMATION

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Gene name

RNF213

Gene description

Ring finger protein 213

Protein class

Cancer-related genes
Disease related genes
Plasma proteins
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

4
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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

General cytoplasmic expression.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 2 antibodies.
HPA003347 , HPA026790
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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

Urinary bladder

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

RNF213 (HGNC Symbol)

Synonyms

C17orf27, KIAA1554, KIAA1618, MYMY2, NET57

Description

Ring finger protein 213 (HGNC Symbol)

Entrez gene summary

This gene encodes a protein containing a C3HC4-type RING finger domain, which is a specialized type of Zn-finger that binds two atoms of zinc and is thought to be involved in mediating protein-protein interactions. The protein also contains an AAA domain, which is associated with ATPase activity. This gene is a susceptibility gene for Moyamoya disease, a vascular disorder of intracranial arteries. This gene is also a translocation partner in anaplastic large cell lymphoma and inflammatory myofibroblastic tumor cases, where a t(2;17)(p23;q25) translocation has been identified with the anaplastic lymphoma kinase (ALK) gene on chromosome 2, and a t(8;17)(q24;q25) translocation has been identified with the MYC gene on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]

Chromosome

17

Cytoband

q25.3

Chromosome location (bp)

80260866 - 80398786

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000173821 (version 78.38)

Entrez gene

57674

UniProt

Q63HN8 (UniProt - Evidence at protein level)

neXtProt

NX_Q63HN8

Antibodypedia

RNF213 antibodies


PROTEIN BROWSER

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ENST00000319921
 
ENST00000508628
 
ENST00000573038
 
ENST00000582970
 
 
 
 


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)

RNF213-001 ENSP00000425956
ENST00000508628
Show » Show » 5256 596.5 No 3
RNF213-002 ENSP00000324392
ENST00000319921
Q63HN8
Show all »
Show » Show » 1063 118.4 No 0
RNF213-015 ENSP00000460462
ENST00000573038
Show » 106 11.7 No 0
RNF213-020 ENSP00000464087
ENST00000582970
Show » Show » 5207 591.4 No 3