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: Ssr3 ENSRNOG00000011148

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Description

signal sequence receptor subunit 3 [Source:RGD Symbol;Acc:621630]

Location

Primary_assembly 2: 151,906,149-151,935,170 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 218 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000014912.8	Ssr3-201	2933	185aa	ENSRNOP00000014912.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J5J5 F1M7T6 Q08013	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,
ENSRNOT00000128232.1	Ssr3-202	1553	173aa	ENSRNOP00000101316.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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