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: pax1b ENSDARG00000073814

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Description

paired box 1 [Source:HGNC Symbol;Acc:HGNC:8615]

Location

Chromosome 20: 48,694,056-48,701,593 reverse strand.

GRCz11:CM002904.2

About this gene

This gene has 3 transcripts (splice variants), 150 orthologues, 56 paralogues and is associated with 14 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000185195.1	pax1b-203	3407	353aa	ENSDARP00000146188.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSDART00000184898.1	pax1b-202	4794	337aa	ENSDARP00000146219.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSDART00000132835.2	pax1b-201	1659	340aa	ENSDARP00000121471.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0S7C8	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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