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

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Gene: efhd2 ENSDARG00000055759

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Description

EF-hand domain family, member D2 [Source:ZFIN;Acc:ZDB-GENE-060531-152]

Location

Chromosome 8: 25,818,622-25,846,188 reverse strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 177 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000128829.3	efhd2-202	1576	233aa	ENSDARP00000108177.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1LVD7	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 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,
ENSDART00000047008.7	efhd2-201	3101	233aa	ENSDARP00000047007.5	Nonsense mediated decay	Q1LVD7	-

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Summary

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