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
External references
Supporting evidence
ID History
- Gene history

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Gene: pnx ENSDARG00000025899

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Description

posterior neuron-specific homeobox [Source:ZFIN;Acc:ZDB-GENE-030328-42]

Location

Chromosome 10: 2,799,285-2,801,857 forward strand.

GRCz11:CM002894.2

About this gene

This gene has 1 transcript (splice variant), 87 orthologues, 16 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000030709.6	pnx-201	837	182aa	ENSDARP00000034835.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R2J1	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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