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

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Gene: VSIG8 ENSOCUG00000002342

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Description

V-set and immunoglobulin domain containing 8 [Source:HGNC Symbol;Acc:HGNC:32063]

Location

Chromosome 13: 33,265,488-33,279,773 forward strand.

OryCun2.0:CM000802.1

About this gene

This gene has 1 transcript (splice variant), 120 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000002342.4	VSIG8-201	1416	471aa	ENSOCUP00000002021.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1SHC2	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,

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Summary

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