Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Efhc2 ENSMUSG00000025038

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Description

EF-hand domain (C-terminal) containing 2 [Source:MGI Symbol;Acc:MGI:1921655]

Gene Synonyms

4933407D04Rik, mRib72-2

Location

Chromosome X: 16,998,278-17,186,211 reverse strand.

GRCm39:CM001013.3

About this gene

This gene has 3 transcripts (splice variants), 195 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000026014.8	Efhc2-201	2554	750aa	ENSMUSP00000026014.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS40883	Q059K2 Q9D485	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000481374.1	Efhc2-202	2373	105aa	ENSMUSP00000259737.1	Nonsense mediated decay		-	-
ENSMUST00000481375.1	Efhc2-203	2372	339aa	ENSMUSP00000259738.1	Nonsense mediated decay		-	-

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Summary

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