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

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Gene: foxn2b ENSDARG00000045105

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Description

forkhead box N2b [Source:ZFIN;Acc:ZDB-GENE-050417-1]

Gene Synonyms

zgc:110577

Location

Chromosome 12: 24,796,517-24,832,297 reverse strand.

GRCz11:CM002896.2

About this gene

This gene has 3 transcripts (splice variants), 145 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000066317.6	foxn2b-201	1728	388aa	ENSDARP00000066316.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q6L3	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,
ENSDART00000185517.1	foxn2b-203	3482	388aa	ENSDARP00000155953.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q6L3	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,
ENSDART00000140262.2	foxn2b-202	575	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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