Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Vsig8 ENSRNOG00000008668

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Description

V-set and immunoglobulin domain containing 8 [Source:RGD Symbol;Acc:1562464]

Gene Synonyms

LOC289236, RGD1562464

Location

Primary_assembly 13: 87,555,533-87,563,720 forward strand.

GRCr8:CM070403.1

About this gene

This gene has 1 transcript (splice variant), 120 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000011539.6	Vsig8-201	1812	417aa	ENSRNOP00000011539.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JG66 D4A7V8	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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Summary

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