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

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Gene: rgs9a ENSDARG00000037925

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Description

regulator of G protein signaling 9a [Source:ZFIN;Acc:ZDB-GENE-060929-92]

Gene Synonyms

rgs9, zgc:152760

Location

Chromosome 3: 36,366,053-36,403,234 forward strand.

GRCz11:CM002887.2

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and 31 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000181140.1	rgs9a-203	3935	480aa	ENSDARP00000157261.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8QUQ1	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,
ENSDART00000151203.3	rgs9a-202	1107	324aa	ENSDARP00000125686.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3IS22	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000150943.2	rgs9a-201	700	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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