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

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Gene: Prss39 ENSRNOG00000023858

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Description

protease, serine, 39 [Source:RGD Symbol;Acc:1309276]

Gene Synonyms

LOC102554718, LOC363215, Prss40, Tesp1, Tesp2

Location

Primary_assembly 9: 36,707,328-36,713,001 forward strand.

mRatBN7.2:CM026982.1

About this gene

This gene has 1 transcript (splice variant), 392 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000034214.5	Prss39-201	1568	369aa	ENSRNOP00000038053.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6AXZ6	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,

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Summary

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