Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
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Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
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Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Sprn ENSRNOG00000067971

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Description

shadow of prion protein [Source:RGD Symbol;Acc:1561845]

Location

Primary_assembly 1: 194,943,826-194,948,460 reverse strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 1 transcript (splice variant), 59 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116404.1	Sprn-201	3768	147aa	ENSRNOP00000094166.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5BIV7	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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