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

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Gene: tp53i11a ENSDARG00000069430

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Description

tumor protein p53 inducible protein 11a [Source:ZFIN;Acc:ZDB-GENE-050306-58]

Gene Synonyms

trp53i11a, zgc:113403

Location

Chromosome 7: 26,649,319-26,704,609 forward strand.

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants), 154 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000101053.6	tp53i11a-201	1999	186aa	ENSDARP00000091827.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6NXK9	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,
ENSDART00000173823.2	tp53i11a-202	799	186aa	ENSDARP00000142773.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6NXK9	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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