Gene: Cpn1 ENSMUSG00000025196

Description

carboxypeptidase N, polypeptide 1 [Source:MGI Symbol;Acc:MGI:2135874]

Gene Synonyms

0610011F20Rik, 50 kDa, CPN

Location

Chromosome 19: 43,944,746-43,974,995 reverse strand.

GRCm39:CM001012.3

About this gene

This gene has 2 transcripts (splice variants), 194 orthologues, 7 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000026210.5	Cpn1-201	1828	457aa	ENSMUSP00000026210.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS29840	Q9JJN5	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, 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,
ENSMUST00000131882.2	Cpn1-202	2212	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	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,

Gene: Cpn1 ENSMUSG00000025196

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Gene: Cpn1 ENSMUSG00000025196

Summary

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