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

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Gene: PAX9 ENSPTRG00000006281

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Description

paired box 9 [Source:VGNC Symbol;Acc:VGNC:57256]

Location

Chromosome 14: 20,635,518-20,653,827 forward strand.

Pan_tro_3.0:CM000328.3

About this gene

This gene has 2 transcripts (splice variants), 201 orthologues and 58 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000011512.6	PAX9-202	1044	347aa	ENSPTRP00000010655.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2Q872	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,
ENSPTRT00000077320.1	PAX9-201	4981	341aa	ENSPTRP00000065976.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8MI71 Q2VL62	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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