Gene: Rnase12 ENSMUSG00000068407

Description

ribonuclease, RNase A family, 12 (non-active) [Source:MGI Symbol;Acc:MGI:3528588]

Location

Chromosome 14: 51,294,155-51,295,118 reverse strand.

GRCm39:CM001007.3

About this gene

This gene has 2 transcripts (splice variants), 69 orthologues, 18 paralogues and is associated with 13 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000227764.2	Rnase12-202	673	145aa	ENSMUSP00000154201.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27032	Q5GAM8 W0UUY1	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,
ENSMUST00000089798.3	Rnase12-201	545	145aa	ENSMUSP00000087231.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27032	Q5GAM8 W0UUY1	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 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,

Gene: Rnase12 ENSMUSG00000068407

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Gene: Rnase12 ENSMUSG00000068407

Summary

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