Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Vil1 ENSRNOG00000015408

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Description

villin 1 [Source:RGD Symbol;Acc:1307048]

Gene Synonyms

LOC316521, Vil

Location

Primary_assembly 9: 83,440,248-83,467,961 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 1 transcript (splice variant), 164 orthologues, 7 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000021432.7	Vil1-201	3301	827aa	ENSRNOP00000021432.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JVU7 F7F8Y1	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Paralogues

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Personal Data