Misplaced Pages

Villin 1

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Protein-coding gene in the species Homo sapiens
VIL1
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1UNC, 3FG7

Identifiers
AliasesVIL1, D2S1471, VIL, villin 1
External IDsOMIM: 193040; MGI: 98930; HomoloGene: 5169; GeneCards: VIL1; OMA:VIL1 - orthologs
Gene location (Human)
Chromosome 2 (human)
Chr.Chromosome 2 (human)
Chromosome 2 (human)Genomic location for VIL1Genomic location for VIL1
Band2q35Start218,419,121 bp
End218,453,295 bp
Gene location (Mouse)
Chromosome 1 (mouse)
Chr.Chromosome 1 (mouse)
Chromosome 1 (mouse)Genomic location for VIL1Genomic location for VIL1
Band1 C3|1 38.54 cMStart74,448,535 bp
End74,474,718 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • jejunal mucosa

  • mucosa of ileum

  • mucosa of transverse colon

  • rectum

  • duodenum

  • mucosa of sigmoid colon

  • buccal mucosa cell

  • gallbladder

  • secondary oocyte

  • islet of Langerhans
Top expressed in
  • ileum

  • intestinal villus

  • epithelium of small intestine

  • Ileal epithelium

  • crypt of lieberkuhn of small intestine

  • colon

  • left colon

  • duodenum

  • jejunum

  • Paneth cell
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

7429

22349

Ensembl

ENSG00000127831

ENSMUSG00000026175

UniProt

P09327

Q62468

RefSeq (mRNA)

NM_007127

NM_009509

RefSeq (protein)

NP_009058

NP_033535

Location (UCSC)Chr 2: 218.42 – 218.45 MbChr 1: 74.45 – 74.47 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Villin 1 is a protein that in humans is encoded by the VIL1 gene. <ref name="entrez {{cite web | title = Entrez Gene: Villin 1 | url = https://www.ncbi.nlm.nih.gov/gene/7429 | access-date = 2018-09-27 }}</ref>

Function

This gene encodes a member of a family of calcium-regulated actin-binding proteins. This protein represents a dominant part of the brush border cytoskeleton which functions in the capping, severing, and bundling of actin filaments. Two mRNAs of 2.7 kb and 3.5 kb have been observed; they result from utilization of alternate poly-adenylation signals present in the terminal exon. .

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000127831Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000026175Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


Stub icon

This article on a gene on human chromosome 2 is a stub. You can help Misplaced Pages by expanding it.

Categories: