Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Gene families
Literature
Metazoan Compara
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Pan-taxonomic Compara
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Genetic Variation
- Variant table
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- Structural variants
Gene expression
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External references
Supporting evidence
ID History
- Gene history

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DB built by FlyBase

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Gene: Efhc1.1 FBgn0030691

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Description

EF-hand domain containing 1.1

Gene Synonyms

Location

Primary_assembly X: 15,780,398-15,783,710 reverse strand.

BDGP6.32:AE014298.5

About this gene

This gene has 1 transcript (splice variant), 112 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
Efhc1.1-RA	FBtr0074192	2559	793aa	FBpp0073977	Gene/transcipt that contains an open reading frame (ORF).Protein coding	C1C543 Q29QV7 Q9VXP5	NM_132847 NM_132847.2 NP_573075 NP_573075.1	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,

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Summary

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Gene-based displays