Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: SRSF9 ENSPTRG00000005535

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Description

serine and arginine rich splicing factor 9 [Source:VGNC Symbol;Acc:VGNC:14417]

Location

Chromosome 12: 123,702,757-123,711,584 reverse strand.

Pan_tro_3.0:CM000326.3

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000010157.4	SRSF9-201	1208	221aa	ENSPTRP00000009392.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XXJ5 H2Q712	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,
ENSPTRT00000108621.1	SRSF9-202	360	119aa	ENSPTRP00000061951.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RBD5 A0A6D2Y188	-

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Summary

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