Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Gprin2 ENSMUSG00000071531

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Description

G protein regulated inducer of neurite outgrowth 2 [Source:MGI Symbol;Acc:MGI:2444560]

Gene Synonyms

C130040D06Rik

Location

Chromosome 14: 33,907,645-33,923,610 reverse strand.

GRCm39:CM001007.3

About this gene

This gene has 3 transcripts (splice variants), 104 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000226613.2	Gprin2-203	10354	455aa	ENSMUSP00000154640.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS49443	A0A2I3BRN2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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,
ENSMUST00000226511.2	Gprin2-202	438	132aa	ENSMUSP00000154257.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A2I3BQP8	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000096019.4	Gprin2-201	430	19aa	ENSMUSP00000093718.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding		D3Z1D7	TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:2, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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