人类

ROR2 - Receptor Tyrosine Kinase Like Orphan Receptor 2

Alias:
BDB
BDB1
NTRKR2
Favorite
Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码的蛋白质是一种属于细胞表面受体ROR亚家族的受体酪氨酸激酶和I型跨膜蛋白质。该蛋白质可能参与早期软骨细胞的形成,并可能对软骨和生长板发育是必需的。这个基因的突变可能导致Brachydactyly Type B,这是一种以远端指骨和指甲发育不全/缺如为特征的骨骼紊乱。此外,这个基因的突变还可能导致Robinow综合征的常染色体隐性形式,其特征是骨骼发育异常,全身四肢骨缩短,脊柱节段缺陷,短手和异常面部外观。[由RefSeq,2008年7月提供]

Basic Information

NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
10
9
227628 bp
104.76
559
2
10
13

ROR2 Genetics information (-)

GRCh38

Sequence Homology

Related Diseases and Mutations

#
Disease
Anatomical Category
Score
Mutations
No data available

Transcripts & Proteins

Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
No data available
* This data comes from NCBI.

Gene Expression

Tissue-specific RNA expression

Organ
Abundance
Alphabetical

Cell-specific RNA expression

Organ
Abundance
Alphabetical

Interactions

Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
No data available

Related Mouse Models

Type
Name
MGI
Strain of Origin
Publications
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
Link
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Mutation Direct
Sequence
Comparison
Al agent
Tutorials
Back to top