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

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Gene: TP73 ENSSSCG00000025685

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Description

tumor protein p73 [Source:VGNC Symbol;Acc:VGNC:94331]

Location

Primary_assembly 6: 65,182,456-65,228,990 forward strand.

Sscrofa11.1:CM000817.5

About this gene

This gene has 5 transcripts (splice variants), 194 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000028860.4	TP73-204	2781	640aa	ENSSSCP00000025975.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0PLG7 I3LPE8	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSSSCT00000077657.2	TP73-203	2847	501aa	ENSSSCP00000062946.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QFG5 A0A8D1DMV0	-
ENSSSCT00000089037.2	TP73-201	2717	590aa	ENSSSCP00000073194.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RA52 A0A8D1DLV0	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSSSCT00000090126.2	TP73-205	2493	544aa	ENSSSCP00000071510.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2R342 A0A8D1DMT7	-
ENSSSCT00000073204.2	TP73-202	1363	405aa	ENSSSCP00000063240.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QHC9 A0A8D1K4A0	-

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data