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: TP53INP1 ENSBTAG00000055158

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Description

tumor protein p53 inducible nuclear protein 1 [Source:VGNC Symbol;Acc:VGNC:36236]

Location

Primary_assembly 14: 69,398,238-69,412,215 forward strand.

ARS-UCD1.3:CM008181.2

About this gene

This gene has 2 transcripts (splice variants), 196 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000084811.2	TP53INP1-202	5977	240aa	ENSBTAP00000071356.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MBC1	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,
ENSBTAT00000090513.1	TP53INP1-201	778	164aa	ENSBTAP00000099179.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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