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

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Gene: PAX9 ENSBTAG00000009186

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Description

paired box 9 [Source:VGNC Symbol;Acc:VGNC:32600]

Location

Primary_assembly 21: 46,863,352-46,877,497 forward strand.

ARS-UCD1.3:CM008188.2

About this gene

This gene has 2 transcripts (splice variants), 202 orthologues and 52 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000012105.6	PAX9-201	1621	361aa	ENSBTAP00000012105.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MFP5	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,
ENSBTAT00000116800.1	PAX9-202	1232	342aa	ENSBTAP00000099410.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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