Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: cnot9 ENSDARG00000033855

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Description

CCR4-NOT transcription complex subunit 9 [Source:NCBI gene;Acc:406632]

Gene Synonyms

rqcd1, wu:fb52b11, wu:fb74e08, zgc:85618

Location

Chromosome 22: 12,752,286-12,763,350 reverse strand.

GRCz11:CM002906.2

About this gene

This gene has 1 transcript (splice variant) and 245 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000143574.2	cnot9-201	1420	298aa	ENSDARP00000113790.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6NWL4	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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