VIM

Gene Information
 
Gene Symbol
VIM
 
Aliases
-
 
Entrez Gene ID
 
Gene Name
Vimentin
 
Chromosomal Location
10p13
 
HGNC ID
 
Summary
This gene encodes a type III intermediate filament protein. Intermediate filaments, along with microtubules and actin microfilaments, make up the cytoskeleton. The encoded protein is responsible for maintaining cell shape and integrity of the cytoplasm, and stabilizing cytoskeletal interactions. This protein is involved in neuritogenesis and cholesterol transport and functions as an organizer of a number of other critical proteins involved in cell attachment, migration, and signaling. Bacterial and viral pathogens have been shown to attach to this protein on the host cell surface. Mutations in this gene are associated with congenital cataracts in human patients. [provided by RefSeq, Aug 2017]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0032967 Biological process Positive regulation of collagen biosynthetic process IMP 21746880
GO:0043488 Biological process Regulation of mRNA stability IMP 21746880
GO:0045727 Biological process Positive regulation of translation IMP 21746880
GO:0071222 Biological process Cellular response to lipopolysaccharide IMP 27812135
GO:0071225 Biological process Cellular response to muramyl dipeptide IMP 27812135
Protein Information
 
Protein Name
Vimentin, epididymis secretory sperm binding protein
 
Function
Vimentins are class-III intermediate filaments found in various non-epithelial cells, especially mesenchymal cells. Vimentin is attached to the nucleus, endoplasmic reticulum, and mitochondria, either laterally or terminally. .; Involved with LARP6 in the stabilization of type I collagen mRNAs for CO1A1 and CO1A2.
 
Refseq Proteins
 
UniProt
 
PDB
Pathways
 
KEGG
 
Reactome
 

Epstein-Barr virus infection
MicroRNAs in cancer

 

Caspase-mediated cleavage of cytoskeletal proteins
Striated Muscle Contraction
Interleukin-4 and Interleukin-13 signaling
Aggrephagy

Interactions
 
STRING MINT IntAct
ENSP00000279804 Q16619
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Cardiovascular Diseases
Acute Coronary Syndrome
Digestive System Diseases
Liver Diseases
Liver Cirrhosis
Hepatitis
Liver Fibrosis
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
PGR, MMP2, MMP9,KRT8 
Endometrial Decidualization  
 
Rotterdam Criteria 
Direct 
10 PCO patients and 10 Non-PCOS  
Metformin alleviated EP-induced decidualization of endometrial stromal cells by modulating secretion of multiple cytokines, inhibiting expression of MMP-2 and MMP-9, activating p38-MAPK signaling and reducing PGR expression, providing a deep insight into the molecular basis of metfromin therapy for PCOS patients 

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