Gene: Efhb ENSMUSG00000023931

Description

EF hand domain family, member B [Source:MGI Symbol;Acc:MGI:3045296]

Gene Synonyms

4921525D22Rik

Location

GRCm39:CM001010.3

About this gene

This gene has 2 transcripts (splice variants), 137 orthologues, 2 paralogues and is associated with 6 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000024725.5	Efhb-201	2661	853aa	ENSMUSP00000024725.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS37652	Q8CDU5	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,
ENSMUST00000233544.2	Efhb-202	3656	290aa	ENSMUSP00000156438.2	Nonsense mediated decay		A0A3B2WCC2	-

Summary