Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SRSF12 ENSSSCG00000032781

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Description

serine and arginine rich splicing factor 12 [Source:VGNC Symbol;Acc:VGNC:93474]

Location

Primary_assembly 1: 57,148,582-57,165,689 reverse strand.

Sscrofa11.1:CM000812.5

About this gene

This gene has 1 transcript (splice variant), 160 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000039409.2	SRSF12-201	890	262aa	ENSSSCP00000047651.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AU64 A0A8D1NZL1	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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