Home
Toolbox
Resource
Workflow
Tutorials
Citations
Downloads
Mutation Al-Predictor Flow
Gene-to-Mutation Flow
News & Insights
Genetic Encyclopedia
Frontiers
Industry Insights
Case Studies
About Us
About the Site
Contact Us
Private Policy
User Agreement
COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
Log In
|
Sign Up
中文
人类
PIN1 - Peptidylprolyl Cis/trans Isomerase, NIMA-interacting 1
Alias:
DOD
UBL5
Create a favorites folder
Cancel
Confirm
Add To Favorites
Select a favorites
Description
New favorites >>
Cancel
Confirm
Favorite
Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
肽基-脯氨酰顺/反异构酶(PPIases)催化肽基-脯氨酰肽键的顺/反异构化。这个基因编码一种特定的PPIase,它可以与磷酸化的ser/thr-pro基序结合,以催化调节其底物的磷酸化后构象。这个PPIase催化的构象调节对参与细胞生长调节、基因毒性和其他应激反应、免疫反应、多能性诱导和维护、生殖细胞发育、神经元分化和生存的关键蛋白具有深远影响。这个酶在阿尔茨海默病和许多癌症的病理发生中也扮演关键角色。这个基因发现有多种可变剪接转录变异体。[RefSeq,2011年6月提供]
Related ID:
NCBI:5300
ENSEMBL:ENSG00000127445
HGNC:8988
UNIPROT:Q13526
OMIM:601052
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
5300
2
4
14372 bp
18.24
5
--
8
21
PIN1 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
Reset
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