Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
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: RP9 ENSBTAG00000032598

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Description

RP9 pre-mRNA splicing factor [Source:VGNC Symbol;Acc:VGNC:34093]

Location

Primary_assembly 4: 63,733,525-63,746,282 forward strand.

ARS-UCD2.0:CM008171.2

About this gene

This gene has 2 transcripts (splice variants) and 152 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000046264.5	RP9-202	1411	329aa	ENSBTAP00000043581.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MEU0	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,
ENSBTAT00000083842.3	RP9-201	1607	328aa	ENSBTAP00000062303.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N0P4	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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