Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- 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: Prss8 ENSRNOG00000019616

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Description

serine protease 8 [Source:RGD Symbol;Acc:619973]

Gene Synonyms

CAP1

Location

Primary_assembly 1: 191,966,701-191,971,193 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 105 orthologues, 1 paralogue and is associated with 12 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026572.8	Prss8-201	2280	374aa	ENSRNOP00000026572.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MA37	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,
ENSRNOT00000094049.2	Prss8-202	2166	336aa	ENSRNOP00000086587.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A1I1	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,
ENSRNOT00000103493.2	Prss8-203	1922	321aa	ENSRNOP00000080070.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZPB9	-

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Summary

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