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Aliases for VIM Gene

Aliases for VIM Gene

External Ids for VIM Gene

Previous GeneCards Identifiers for VIM Gene

  • GC10P017253
  • GC10P017421
  • GC10P017275
  • GC10P017310
  • GC10P017270

Summaries for VIM Gene

Entrez Gene Summary for VIM Gene

  • 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]

GeneCards Summary for VIM Gene

VIM (Vimentin) is a Protein Coding gene. Diseases associated with VIM include Cataract 30, Pulverulent and Malignant Mixed Mullerian Tumor. Among its related pathways are DNA Damage and Cytoskeleton remodeling Neurofilaments. GO annotations related to this gene include identical protein binding and protein C-terminus binding. An important paralog of this gene is DES.

UniProtKB/Swiss-Prot for VIM Gene

  • 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.

Gene Wiki entry for VIM Gene

Additional gene information for VIM Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for VIM Gene

Genomics for VIM Gene

Regulatory Elements for VIM Gene

Enhancers for VIM Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH10H017212 2 FANTOM5 Ensembl ENCODE dbSUPER 28.7 -12.0 -11951 7.7 PKNOX1 FOXA2 ATF1 ARNT TCF12 ZNF766 ATF7 FOS RUNX3 SP3 VIM CUBN VIM-AS1 TRDMT1
GH10H017021 1.9 FANTOM5 Ensembl ENCODE dbSUPER 20.8 -201.8 -201846 9.6 PKNOX1 ATF1 ARNT TCF12 CBX5 GATA2 FOS ATF7 RUNX3 CAVIN1 VIM CUBN ENSG00000234961 TRDMT1 GC10P016843
GH10H016999 1.9 FANTOM5 Ensembl ENCODE dbSUPER 20 -222.7 -222687 11.8 PKNOX1 ATF1 ARNT ZNF133 FEZF1 TCF12 ZNF766 GATA2 ELK1 FOS VIM LOC105376438 ENSG00000234961 CUBN RSU1 TRDMT1 ST8SIA6 GC10P016843
GH10H017073 1.6 FANTOM5 Ensembl ENCODE dbSUPER 18.1 -151.8 -151814 4.8 L3MBTL2 TAL1 JUN CEBPB CEBPG EP300 JUND POLR2A CREB1 FOS VIM CUBN TRDMT1 GC10P016843
GH10H017664 1.5 FANTOM5 Ensembl ENCODE dbSUPER 16 +437.9 437856 2.4 JUN USF2 CEBPB CEBPG EP300 NR2F2 FOSL1 JUND FOS KDM1A VIM STAM ST8SIA6 LOC105376438
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around VIM on UCSC Golden Path with GeneCards custom track

Promoters for VIM Gene
Ensembl Regulatory Elements (ENSRs) TSS Distance (bp) Size (bp) Binding Sites for Transcription Factors within promoters
ENSR00000025091 1965 5001 HDGF PKNOX1 ARNT SIN3A FEZF1 ZNF2 ZNF766 ZNF143 ZNF207 FOS

Genomic Locations for VIM Gene

Genomic Locations for VIM Gene
9,659 bases
Plus strand

Genomic View for VIM Gene

Genes around VIM on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
VIM Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for VIM Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for VIM Gene

Proteins for VIM Gene

  • Protein details for VIM Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Protein Accession:
    Secondary Accessions:
    • B0YJC2
    • D3DRU4
    • Q15867
    • Q15868
    • Q15869
    • Q548L2
    • Q6LER9
    • Q8N850
    • Q96ML2
    • Q9NTM3

    Protein attributes for VIM Gene

    466 amino acids
    Molecular mass:
    53652 Da
    Quaternary structure:
    • Homopolymer assembled from elementary dimers. Interacts with HCV core protein (PubMed:15846844). Interacts with LGSN and SYNM. Interacts (via rod region) with PLEC (via CH 1 domain) (By similarity). Interacts with SLC6A4 (PubMed:19270731). Interacts with STK33 (PubMed:18811945). Interacts with LARP6 (PubMed:21746880). Interacts with RAB8B (By similarity). Interacts with TOR1A; the interaction associates TOR1A with the cytoskeleton (PubMed:16361107, PubMed:18827015). Interacts with TOR1AIP1 (PubMed:16361107). Interacts with BCAS3 (PubMed:17505058). Interacts with DIAPH1 (PubMed:23325789). Identified in complexes that contain VIM, EZR, AHNAK, BFSP1, BFSP2, ANK2, PLEC, PRX and spectrin (By similarity). Interacts with EPPK1; interaction is dependent of higher-order structure of intermediate filament (PubMed:16923132).
    • Sequence=BAB71275.1; Type=Miscellaneous discrepancy; Note=Product of a cloning artifact.; Evidence={ECO:0000305};

    Three dimensional structures from OCA and Proteopedia for VIM Gene

neXtProt entry for VIM Gene

Post-translational modifications for VIM Gene

  • Filament disassembly during mitosis is promoted by phosphorylation at Ser-55 as well as by nestin (By similarity). One of the most prominent phosphoproteins in various cells of mesenchymal origin. Phosphorylation is enhanced during cell division, at which time vimentin filaments are significantly reorganized. Phosphorylation by PKN1 inhibits the formation of filaments. Phosphorylated at Ser-56 by CDK5 during neutrophil secretion in the cytoplasm. Phosphorylated by STK33.
  • O-glycosylated during cytokinesis at sites identical or close to phosphorylation sites, this interferes with the phosphorylation status.
  • S-nitrosylation is induced by interferon-gamma and oxidatively-modified low-densitity lipoprotein (LDL(ox)) possibly implicating the iNOS-S100A8/9 transnitrosylase complex.
  • Ubiquitination at Lys97, posLast=120120, Lys129, Lys139, Lys168, Lys188, posLast=236236, posLast=282282, posLast=294294, posLast=313313, posLast=373373, and posLast=445445
  • Glycosylation at Ser7, Thr33, and posLast=3434
  • Modification sites at PhosphoSitePlus

Other Protein References for VIM Gene

Antibody Products

  • Cell Signaling Technology (CST) Antibodies for VIM (Vimentin)

No data available for DME Specific Peptides for VIM Gene

Domains & Families for VIM Gene

Gene Families for VIM Gene

Human Protein Atlas (HPA):
  • Disease related genes
  • Plasma proteins
  • Predicted intracellular proteins

Suggested Antigen Peptide Sequences for VIM Gene

Graphical View of Domain Structure for InterPro Entry



  • The central alpha-helical coiled-coil rod region mediates elementary homodimerization.
  • Belongs to the intermediate filament family.
  • The central alpha-helical coiled-coil rod region mediates elementary homodimerization.
  • The [IL]-x-C-x-x-[DE] motif is a proposed target motif for cysteine S-nitrosylation mediated by the iNOS-S100A8/A9 transnitrosylase complex.
  • Belongs to the intermediate filament family.
genes like me logo Genes that share domains with VIM: view

Function for VIM Gene

Molecular function for VIM Gene

GENATLAS Biochemistry:
vimentin,intermediate filament protein,expressed in cells of mesenchymal origin,regulated by an antisilencer element
UniProtKB/Swiss-Prot 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.
UniProtKB/Swiss-Prot Function:
Involved with LARP6 in the stabilization of type I collagen mRNAs for CO1A1 and CO1A2.

Phenotypes From GWAS Catalog for VIM Gene

Gene Ontology (GO) - Molecular Function for VIM Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0003725 double-stranded RNA binding IDA 21266579
GO:0005198 structural molecule activity IEA --
GO:0005200 structural constituent of cytoskeleton IDA 11889032
GO:0005212 structural constituent of eye lens IEA --
GO:0005515 protein binding IPI 10852826
genes like me logo Genes that share ontologies with VIM: view
genes like me logo Genes that share phenotypes with VIM: view

Human Phenotype Ontology for VIM Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for VIM Gene

MGI Knock Outs for VIM:

Clone Products

  • Addgene plasmids for VIM

No data available for Enzyme Numbers (IUBMB) , Transcription Factor Targets and HOMER Transcription for VIM Gene

Localization for VIM Gene

Subcellular locations from UniProtKB/Swiss-Prot for VIM Gene


Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for VIM gene
Compartment Confidence
extracellular 5
cytoskeleton 5
peroxisome 5
cytosol 5
mitochondrion 3
nucleus 3
plasma membrane 2

Subcellular locations from the

Human Protein Atlas (HPA)
  • Intermediate filaments (3)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for VIM Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005737 cytoplasm IDA,IEA 9150946
GO:0005777 peroxisome IDA 17881773
GO:0005829 cytosol TAS --
GO:0005856 cytoskeleton TAS,IDA 16130169
GO:0005882 intermediate filament IEA,IDA 11889032
genes like me logo Genes that share ontologies with VIM: view

Pathways & Interactions for VIM Gene

genes like me logo Genes that share pathways with VIM: view

SIGNOR curated interactions for VIM Gene

Is activated by:
Is inactivated by:
Other effect:

Gene Ontology (GO) - Biological Process for VIM Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0006928 movement of cell or subcellular component TAS 16130169
GO:0010628 positive regulation of gene expression IEA --
GO:0010977 negative regulation of neuron projection development IEA --
GO:0014002 astrocyte development IEA --
GO:0016032 viral process IEA --
genes like me logo Genes that share ontologies with VIM: view

Drugs & Compounds for VIM Gene

(88) Drugs for VIM Gene - From: DrugBank, HMDB, and Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Carnosine Investigational Pharma 0
Phenethyl isothiocyanate Investigational Pharma Target 12

(69) Additional Compounds for VIM Gene - From: Novoseek

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
genes like me logo Genes that share compounds with VIM: view

Transcripts for VIM Gene

Unigene Clusters for VIM Gene

Representative Sequences:

Clone Products

  • Addgene plasmids for VIM

Alternative Splicing Database (ASD) splice patterns (SP) for VIM Gene

ExUns: 1 ^ 2 ^ 3a · 3b · 3c ^ 4a · 4b ^ 5 ^ 6 ^ 7 ^ 8a · 8b ^ 9 ^ 10 ^ 11
SP1: - - -
SP4: - -

Relevant External Links for VIM Gene

GeneLoc Exon Structure for
ECgene alternative splicing isoforms for

Expression for VIM Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for VIM Gene

mRNA differential expression in normal tissues according to GTEx for VIM Gene

This gene is overexpressed in Artery - Aorta (x4.3) and Artery - Tibial (x4.2).

Protein differential expression in normal tissues from HIPED for VIM Gene

This gene is overexpressed in Bone marrow stromal cell (17.5) and Adipocyte (9.5).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, MaxQB, and MOPED for VIM Gene

Protein tissue co-expression partners for VIM Gene

NURSA nuclear receptor signaling pathways regulating expression of VIM Gene:


SOURCE GeneReport for Unigene cluster for VIM Gene:


mRNA Expression by UniProt/SwissProt for VIM Gene:

Tissue specificity: Highly expressed in fibroblasts, some expression in T- and B-lymphocytes, and little or no expression in Burkitts lymphoma cell lines. Expressed in many hormone-independent mammary carcinoma cell lines.

Evidence on tissue expression from TISSUES for VIM Gene

  • Blood(5)
  • Liver(5)
  • Lung(5)
  • Skin(5)
  • Nervous system(5)
  • Eye(4.9)
  • Intestine(4.9)
  • Kidney(4.9)
  • Stomach(4.9)
  • Bone(4.8)
  • Heart(4.8)
  • Pancreas(4.7)
  • Spleen(4.7)
  • Thyroid gland(4.6)
  • Muscle(3.8)
  • Bone marrow(3.3)
  • Lymph node(3.1)
  • Adrenal gland(2.8)
  • Gall bladder(2.8)

Phenotype-based relationships between genes and organs from Gene ORGANizer for VIM Gene

Germ Layers:
  • ectoderm
  • nervous
Head and neck:
  • brain
  • cranial nerve
  • eye
  • head
  • peripheral nervous system
genes like me logo Genes that share expression patterns with VIM: view

Orthologs for VIM Gene

This gene was present in the common ancestor of chordates.

Orthologs for VIM Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia VIM 33 34
  • 99.43 (n)
(Monodelphis domestica)
Mammalia VIM 34
  • 95 (a)
(Canis familiaris)
Mammalia VIM 33 34
  • 94.49 (n)
(Bos Taurus)
Mammalia VIM 33 34
  • 92.64 (n)
(Mus musculus)
Mammalia Vim 33 16 34
  • 91.61 (n)
(Rattus norvegicus)
Mammalia Vim 33
  • 91.61 (n)
(Ornithorhynchus anatinus)
Mammalia VIM 34
  • 88 (a)
(Gallus gallus)
  • 89 (a)
VIM 33
  • 83.59 (n)
(Anolis carolinensis)
Reptilia VIM 34
  • 75 (a)
tropical clawed frog
(Silurana tropicalis)
Amphibia vim 33
  • 73.45 (n)
Str.11198 33
African clawed frog
(Xenopus laevis)
Amphibia vim1 33
(Danio rerio)
Actinopterygii vim 33 34
  • 71.83 (n)
viml 34
  • 68 (a)
-- 33
rainbow trout
(Oncorhynchus mykiss)
Actinopterygii Omy.11950 33
Species where no ortholog for VIM was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • fruit fly (Drosophila melanogaster)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)
  • worm (Caenorhabditis elegans)

Evolution for VIM Gene

Gene Tree for VIM (if available)
Gene Tree for VIM (if available)

Paralogs for VIM Gene

Variants for VIM Gene

Sequence variations from dbSNP and Humsavar for VIM Gene

SNP ID Clin Chr 10 pos Sequence Context AA Info Type
rs121917775 Pathogenic, Cataract 30, multiple types (CTRCT30) [MIM:116300] 17,229,873(+) TCTAC(A/G)AGGAG nc-transcript-variant, reference, missense
VAR_078860 Cataract 30, multiple types (CTRCT30) [MIM:116300]
rs864309690 Likely pathogenic 17,229,437(+) AGGTC(-/C)GTGTC nc-transcript-variant, reference, frameshift-variant
rs1000052726 -- 17,228,351(+) AGGGG(A/C)GCTCT intron-variant, upstream-variant-2KB, utr-variant-5-prime
rs1000104769 -- 17,228,140(+) AAAAG(C/T)TGGGT intron-variant, upstream-variant-2KB, utr-variant-5-prime

Structural Variations from Database of Genomic Variants (DGV) for VIM Gene

Variant ID Type Subtype PubMed ID
nsv831801 CNV gain 17160897
nsv508571 CNV deletion 20534489
nsv1039697 CNV loss 25217958
esv2659900 CNV deletion 23128226
dgv179e212 CNV loss 25503493

Variation tolerance for VIM Gene

Residual Variation Intolerance Score: 15.8% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 0.85; 17.70% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for VIM Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for VIM Gene

Disorders for VIM Gene

MalaCards: The human disease database

(167) MalaCards diseases for VIM Gene - From: HGMD, OMIM, ClinVar, GeneTests, Orphanet, Swiss-Prot, DISEASES, Novoseek, and GeneCards

Disorder Aliases PubMed IDs
cataract 30, pulverulent
  • cataract 30
malignant mixed mullerian tumor
  • carcinosarcoma
spindle cell carcinoma
  • sarcomatoid carcinoma
glomus tumor
  • glomus neoplasm
clear cell ependymoma
  • cellular ependymoma
- elite association - COSMIC cancer census association via MalaCards
Search VIM in MalaCards View complete list of genes associated with diseases


  • Cataract 30, multiple types (CTRCT30) [MIM:116300]: An opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. {ECO:0000269 PubMed:19126778, ECO:0000269 PubMed:26694549, ECO:0000269 PubMed:28450710}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Relevant External Links for VIM

Genetic Association Database (GAD)
Human Genome Epidemiology (HuGE) Navigator
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
genes like me logo Genes that share disorders with VIM: view

No data available for Genatlas for VIM Gene

Publications for VIM Gene

  1. The cellular distribution of serotonin transporter is impeded on serotonin-altered vimentin network. (PMID: 19270731) Ahmed BA … Kilic F (PloS one 2009) 3 4 22 60
  2. The Serine/threonine kinase Stk33 exhibits autophosphorylation and phosphorylates the intermediate filament protein Vimentin. (PMID: 18811945) Brauksiepe B … Schmidt ER (BMC biochemistry 2008) 3 4 22 60
  3. Specific in vivo phosphorylation sites determine the assembly dynamics of vimentin intermediate filaments. (PMID: 14762106) Eriksson JE … Goldman RD (Journal of cell science 2004) 3 4 22 60
  4. SEREX identification of new tumour-associated antigens in cutaneous T-cell lymphoma. (PMID: 14996095) Hartmann TB … Eichmüller S (The British journal of dermatology 2004) 3 4 22 60
  5. Cdk5 mediates vimentin Ser56 phosphorylation during GTP-induced secretion by neutrophils. (PMID: 21465480) Lee KY … Rosales JL (Journal of cellular physiology 2012) 3 4 60

Products for VIM Gene

  • Addgene plasmids for VIM

Sources for VIM Gene

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