Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Prr14l ENSRNOG00000048891

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Description

proline rich 14-like [Source:RGD Symbol;Acc:1305469]

Gene Synonyms

LOC305466, RGD1305469

Location

Primary_assembly 14: 82,094,358-82,158,323 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 1 transcript (splice variant), 183 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000072368.4	Prr14l-201	7131	1973aa	ENSRNOP00000066545.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RAJ5	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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