Gene: Atg14 ENSMUSG00000037526

Description

autophagy related 14 [Source:MGI Symbol;Acc:MGI:1261775]

Gene Synonyms

Barkor, D14Ertd114e, D14Ertd436e

Location

Chromosome 14: 47,778,350-47,808,106 reverse strand.

GRCm39:CM001007.3

About this gene

This gene has 4 transcripts (splice variants), 208 orthologues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000226299.2	Atg14-202	3729	492aa	ENSMUSP00000153718.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26989	Q8CDJ3	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,
ENSMUST00000042988.7	Atg14-201	3450	492aa	ENSMUSP00000039047.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26989	Q8CDJ3	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,
ENSMUST00000228784.2	Atg14-204	376	125aa	ENSMUSP00000154124.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A2I3BQC2	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSMUST00000227971.2	Atg14-203	496	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

Gene: Atg14 ENSMUSG00000037526

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Gene: Atg14 ENSMUSG00000037526

Summary

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