Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Vsig1 ENSRNOG00000054219

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Description

V-set and immunoglobulin domain containing 1 [Source:RGD Symbol;Acc:1565570]

Gene Synonyms

LOC315920, MGC114516

Location

Primary_assembly X: 109,395,035-109,428,624 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants), 165 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000091441.3	Vsig1-202	2439	440aa	ENSRNOP00000073037.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K4G7	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,
ENSRNOT00000082652.3	Vsig1-201	2901	404aa	ENSRNOP00000075185.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HLR1 Q4KLY3	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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