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

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Gene: Prb1 ENSRNOG00000010449

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Description

proline-rich protein BstNI subfamily 1 [Source:RGD Symbol;Acc:628796]

Gene Synonyms

Prpg1

Location

Primary_assembly 4: 167,240,337-167,243,803 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant) and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000013887.7	Prb1-201	752	207aa	ENSRNOP00000013885.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IMA3 F1LMA2	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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