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: pax9 ENSDARG00000053829

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Description

paired box 9 [Source:NCBI gene (formerly Entrezgene);Acc:30558]

Location

Chromosome 17: 38,236,469-38,291,065 reverse strand.

GRCz11:CM002901.2

About this gene

This gene has 3 transcripts (splice variants), 197 orthologues, 56 paralogues and is associated with 17 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000075936.7	pax9-202	1903	343aa	ENSDARP00000070415.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q98865	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,
ENSDART00000075932.6	pax9-201	1763	270aa	ENSDARP00000070411.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q98866	-
ENSDART00000152056.2	pax9-203	759	15aa	ENSDARP00000126510.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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