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: Ssna1 ENSRNOG00000011093

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Description

SS nuclear autoantigen 1 [Source:RGD Symbol;Acc:1310259]

Gene Synonyms

LOC311802

Location

Primary_assembly 3: 28,483,107-28,484,608 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants), 116 orthologues and is associated with 8 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000119530.2	Ssna1-202	1139	158aa	ENSRNOP00000090440.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACI2	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,
ENSRNOT00000014993.8	Ssna1-201	929	119aa	ENSRNOP00000014993.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A9K3Y6S6 B2RZ20	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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