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
  - Gene tree
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Ontologies
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Genetic Variation
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Gene expression
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External references
Supporting evidence
ID History
- Gene history

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Gene: Prnd ENSRNOG00000021260

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Description

prion like protein doppel [Source:RGD Symbol;Acc:1306618]

Location

Primary_assembly 3: 119,213,429-119,218,745 forward strand.

mRatBN7.2:CM026976.1

About this gene

This gene has 2 transcripts (splice variants), 77 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000115601.1	Prnd-202	3303	178aa	ENSRNOP00000088923.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A7U7N4	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,
ENSRNOT00000050900.4	Prnd-201	2437	178aa	ENSRNOP00000039441.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A7U7N4	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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