Gene: Efhb ENSRNOG00000012618

Description

EF hand domain family, member B [Source:RGD Symbol;Acc:1566407]

Gene Synonyms

LOC301168, RGD1566407

Location

GRCr8:CM070399.1

About this gene

This gene has 1 transcript (splice variant), 134 orthologues, 2 paralogues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000016911.8	Efhb-201	3214	986aa	ENSRNOP00000016911.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZTX5	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, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

Summary