Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
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Molecular interactions
External references
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ID History
- Gene history

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Gene: PI16 ENSBTAG00000002092

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Description

peptidase inhibitor 16 [Source:VGNC Symbol;Acc:VGNC:32853]

Location

Primary_assembly 23: 10,861,228-10,875,475 forward strand.

ARS-UCD2.0:CM008190.2

About this gene

This gene has 2 transcripts (splice variants) and 85 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000047585.5	PI16-202	2469	464aa	ENSBTAP00000044778.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q58D34	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 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,
ENSBTAT00000002703.6	PI16-201	2326	433aa	ENSBTAP00000002703.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6YJ25	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,

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Summary

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