Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Prss42 ENSRNOG00000031971

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Description

serine protease 42 [Source:RGD Symbol;Acc:1562548]

Gene Synonyms

LOC301027, RGD1562548, Tessp2

Location

Primary_assembly 8: 119,650,839-119,657,909 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 1 transcript (splice variant), 411 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000051211.6	Prss42-201	3001	385aa	ENSRNOP00000044227.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I3G9 D3ZXU4	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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