Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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Gene: Rpp14 ENSMUSG00000023156

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Description

ribonuclease P 14 subunit [Source:MGI Symbol;Acc:MGI:1914303]

Gene Synonyms

2610511E03Rik

Location

Chromosome 14: 14,377,939-14,389,406 reverse strand.

GRCm39:CM001007.3

About this gene

This gene has 2 transcripts (splice variants) and 172 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000180369.2	Rpp14-202	477	158aa	ENSMUSP00000136494.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		J3QMX0	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL NA: A transcript that was not analysed for TSL. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:NA,
ENSMUST00000023924.4	Rpp14-201	2401	122aa	ENSMUSP00000023924.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26809	Q9CQH8	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

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Summary

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