About   Help   FAQ
Vim Gene Detail
Summary
  • Symbol
    Vim
  • Name
    vimentin
  • Feature Type
    protein coding gene
  • IDs
    MGI:98932
    NCBI Gene: 22352
  • Gene Overview
    MyGene.info: VIM
  • Alliance
    gene page
Location & Maps
more
  • Sequence Map
    Chr2:13573927-13582826 bp, + strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser
  • Download
    Sequence
      8900 bp   ±  kb flank

  • Genome Browsers
    VEGA | Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 2, 10.04 cM, cytoband A2
  • Mapping Data
    24 experiments
  • Sequence Tag
    D2Mit149
Homology
more
  • Human Ortholog
    VIM, vimentin
  • Vertebrate Orthologs
    9
  • Human Ortholog
    VIM, vimentin
    Orthology source: HomoloGene, HGNC
  • Links
    NCBI Gene ID: 7431
    neXtProt AC: NX_P08670
    UniProt: P08670

  • Chr Location
    10p13; chr10:17227935-17237593 (+)  GRCh38.p7
  • HomoloGene
    Vertebrate Homology Class 2538
    1 human;1 mouse;1 rat;1 chimpanzee;1 cattle;1 dog;1 chicken;1 zebrafish;1 frog, western clawed
  • HCOP
    human homology predictions: VIM
  • Gene Tree
    Vim
Human Diseases
more
  • Diseases
    1 with Vim mouse models; 1 with human VIM associations

Human Disease Mouse Models
      
IDs
 View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    39 phenotypes from 3 alleles in 3 genetic backgrounds
    25 phenotypes from multigenic genotypes
    56 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Homozygous null mutants exhibit impaired performance in motor coordination tests; cerebellum shows underdeveloped/abnormal Bergman glia and stunted, poorly branched Purkinje cells. Mutants are unable to survive experimental 75% reduction of kidney mass.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    60
  • GO References
    31
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    278
  • Tissues
    247
  • cDNA Data
    713
  • Literature Summary
    269
  • Comparison Matrix
    Gene Expression + Phenotype
    • Interactions
    less
    Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic OTTMUSG00000011231 VEGA Gene Model | MGI Sequence Detail 8900 C57BL/6J ±  kb
    transcript OTTMUST00000026365 VEGA | MGI Sequence Detail 2193 Not Applicable  
    polypeptide OTTMUSP00000012058 VEGA | MGI Sequence Detail 466 Not Applicable  
    For the selected sequence
    Polymorphisms
    less
    • SNPs within 2kb
      76 from dbSNP Build 142
    • RFLP
      5
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 728
      Genomic 3
      cDNA 717
      Primer pair 5
      Other 3

      Microarray probesets 5
    Other
    Accession IDs
    less
    MGD-MRK-15395
    References
    more
    • Summaries
      All 435
      Developmental Gene Expression 269
      Diseases 1
      Gene Ontology 31
      Phenotypes 56
    • Earliest
      J:29340 Jackson BW, et al., Formation of cytoskeletal elements during mouse embryogenesis. Intermediate filaments of the cytokeratin type and desmosomes in preimplantation embryos. Differentiation. 1980;17(3):161-79
    • Latest
      J:258246 Hosseini ZF, et al., FGF2-dependent mesenchyme and laminin-111 are niche factors in salivary gland organoids. J Cell Sci. 2018 Feb 20;131(4)
    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
    Citing These Resources
    Funding Information
    Warranty Disclaimer & Copyright Notice
    Send questions and comments to User Support.     		last database update
    06/12/2018
    MGI 6.12     		The Jackson Laboratory