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

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Gene: PRR7 ENSSSCG00000040698

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Description

proline rich 7, synaptic [Source:VGNC Symbol;Acc:VGNC:91863]

Location

Primary_assembly 2: 80,496,106-80,505,430 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 1 transcript (splice variant), 124 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000045845.1	PRR7-201	1351	270aa	ENSSSCP00000031845.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZJV2 A0A4X1SEN0	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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