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: VSIG2 ENSBTAG00000022379

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Description

V-set and immunoglobulin domain containing 2 [Source:VGNC Symbol;Acc:VGNC:50036]

Location

Primary_assembly 29: 28,226,459-28,231,754 reverse strand.

ARS-UCD2.0:CM008196.2

About this gene

This gene has 2 transcripts (splice variants), 119 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000074193.2	VSIG2-201	1248	330aa	ENSBTAP00000068542.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MHI0	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,
ENSBTAT00000030293.5	VSIG2-202	1139	329aa	ENSBTAP00000030277.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BL94	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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