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

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Gene: fpr1 ENSDARG00000042984

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Description

formyl peptide receptor 1 [Source:ZFIN;Acc:ZDB-GENE-121227-2]

Location

Chromosome 16: 24,971,717-24,974,700 forward strand.

GRCz11:CM002900.2

About this gene

This gene has 2 transcripts (splice variants), 268 orthologues, 25 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000156958.2	fpr1-202	1921	388aa	ENSDARP00000127715.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	X1WBX3	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000063115.7	fpr1-201	1119	372aa	ENSDARP00000063114.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FF45	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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