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

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Gene: VSNL1 ENSBTAG00000017158

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Description

visinin like 1 [Source:VGNC Symbol;Acc:VGNC:36841]

Location

Primary_assembly 11: 80,940,127-81,060,773 reverse strand.

ARS-UCD2.0:CM008178.2

About this gene

This gene has 2 transcripts (splice variants), 263 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000075460.2	VSNL1-201	1555	195aa	ENSBTAP00000072671.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MET3	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,
ENSBTAT00000022814.5	VSNL1-202	1598	191aa	ENSBTAP00000022814.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P62763	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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Summary

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