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: VSIG1 ENSOCUG00000010826

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Description

V-set and immunoglobulin domain containing 1 [Source:HGNC Symbol;Acc:HGNC:28675]

Location

Chromosome X: 56,658,558-56,694,777 forward strand.

OryCun2.0:CM000811.1

About this gene

This gene has 2 transcripts (splice variants), 165 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000040703.1	VSIG1-201	1221	406aa	ENSOCUP00000033814.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSOCUT00000010826.4	VSIG1-202	1116	371aa	ENSOCUP00000009314.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1T020	-

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Summary

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