Gene: Rnase6 ENSMUSG00000021880

Description

ribonuclease, RNase A family, 6 [Source:MGI Symbol;Acc:MGI:1925666]

Gene Synonyms

9530043P15Rik

Location

Chromosome 14: 51,361,365-51,369,644 forward strand.

GRCm39:CM001007.3

About this gene

This gene has 4 transcripts (splice variants), 91 orthologues, 18 paralogues and is associated with 8 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000226194.2	Rnase6-202	2452	153aa	ENSMUSP00000154125.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27037	Q3V3L3	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, 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,
ENSMUST00000095923.4	Rnase6-201	1072	153aa	ENSMUSP00000093613.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27037	Q3V3L3	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,
ENSMUST00000226210.2	Rnase6-203	422	33aa	ENSMUSP00000154794.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A2I3BS15	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000228752.2	Rnase6-204	418	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-

Gene: Rnase6 ENSMUSG00000021880

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Gene: Rnase6 ENSMUSG00000021880

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