Gene: Trim38 ENSMUSG00000064140

Description

tripartite motif-containing 38 [Source:MGI Symbol;Acc:MGI:2684869]

Gene Synonyms

LOC214158

Location

Chromosome 13: 23,953,896-23,975,511 forward strand.

GRCm39:CM001006.3

About this gene

This gene has 3 transcripts (splice variants), 106 orthologues, 74 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000226039.2	Trim38-203	1999	471aa	ENSMUSP00000153240.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26370	Q5SZ99	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,
ENSMUST00000074067.4	Trim38-201	1480	471aa	ENSMUSP00000073709.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26370	Q5SZ99	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,
ENSMUST00000223911.2	Trim38-202	1457	249aa	ENSMUSP00000153540.2	Nonsense mediated decay		A0A286YDR5	-

Gene: Trim38 ENSMUSG00000064140

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Gene: Trim38 ENSMUSG00000064140

Summary

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