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

Configure this page

Share this page

Bookmark this page

.

Gene: VILL ENSPTRG00000014750

.

Description

villin like [Source:VGNC Symbol;Acc:VGNC:12231]

Location

Chromosome 3: 38,739,713-38,755,336 forward strand.

Pan_tro_3.0:CM000317.3

About this gene

This gene has 2 transcripts (splice variants), 197 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000027585.4	VILL-201	4835	855aa	ENSPTRP00000025438.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8NQA8 A0A6D2VZG8	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,
ENSPTRT00000102760.1	VILL-202	1725	574aa	ENSPTRP00000085675.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T8U6 A0A6D2XR31	-

.

Summary

.

.