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

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Gene: fxr2 ENSDARG00000016260

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Description

FMR1 autosomal homolog 2 [Source:NCBI gene (formerly Entrezgene);Acc:393180]

Gene Synonyms

id:ibd5046, zgc:56215, zgc:77472

Location

Chromosome 7: 22,718,251-22,761,090 forward strand.

GRCz11:CM002891.2

About this gene

This gene has 3 transcripts (splice variants), 193 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSDART00000027718.9	fxr2-201	4106	676aa	ENSDARP00000004667.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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,
ENSDART00000143341.3	fxr2-202	2521	583aa	ENSDARP00000113332.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSDART00000173609.2	fxr2-203	729	160aa	ENSDARP00000142685.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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