ROR2

GENERAL INFORMATION

? »

Gene name

ROR2

Gene description

Receptor tyrosine kinase-like orphan receptor 2

Protein class

Disease related genes
Enzymes
Potential drug targets
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

2
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Mixed
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Moderate to strong cytoplasmic immunoreactivity, often with membranous positivity, was observed in normal tissues. Gastrointestinal tract, exocrine pancreas, placenta, male genitalia and Purkinje cells showed strong positivity. Hepatocytes were negative.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA021868
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
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



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

? »

Gene name

ROR2 (HGNC Symbol)

Synonyms

BDB, BDB1, NTRKR2

Description

Receptor tyrosine kinase-like orphan receptor 2 (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008]

Chromosome

9

Cytoband

q22.31

Chromosome location (bp)

91563091 - 91950162

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000169071 (version 78.38)

Entrez gene

4920

UniProt

Q01974 (UniProt - Evidence at protein level)

neXtProt

NX_Q01974

Antibodypedia

ROR2 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000375708
 
ENST00000375715
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ROR2-001 ENSP00000364860
ENST00000375708
Q01974
Show all »
Show » Show » 943 104.8 Yes 1
ROR2-002 ENSP00000364867
ENST00000375715
B1APY4
Show all »
Show » Show » 704 79.3 No 1