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

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Gene: Pi16 ENSRNOG00000000525

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Description

peptidase inhibitor 16 [Source:RGD Symbol;Acc:1304760]

Gene Synonyms

LOC294312

Location

Primary_assembly 20: 7,377,729-7,387,691 forward strand.

GRCr8:CM070410.1

About this gene

This gene has 3 transcripts (splice variants), 85 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000000632.9	Pi16-201	2904	596aa	ENSRNOP00000000632.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZGM7	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,
ENSRNOT00000149021.1	Pi16-203	2883	581aa	ENSRNOP00000105370.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000093209.3	Pi16-202	1480	352aa	ENSRNOP00000076126.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2Q642	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,

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Summary

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