Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Ssx1 ENSRNOG00000027850

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Description

SSX family member 1 [Source:RGD Symbol;Acc:1593374]

Gene Synonyms

LOC691903

Location

Primary_assembly X: 16,604,449-16,612,210 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues, 1 paralogue and is associated with 11 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000030146.8	Ssx1-201	687	184aa	ENSRNOP00000037344.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M0F5	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,
ENSRNOT00000093905.2	Ssx1-202	557	126aa	ENSRNOP00000087992.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A9U9	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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Paralogues

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