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

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Gene: SRSF9 ENSBTAG00000012792

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Description

serine and arginine rich splicing factor 9 [Source:VGNC Symbol;Acc:VGNC:52832]

Location

Primary_assembly 17: 62,757,004-62,770,204 reverse strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 2 transcripts (splice variants), 210 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000016997.6	SRSF9-201	1011	221aa	ENSBTAP00000016997.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A4FUC6	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,
ENSBTAT00000121906.1	SRSF9-202	906	187aa	ENSBTAP00000086552.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SML6	-

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Summary

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