Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
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Molecular interactions
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ID History
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Gene: Cnot11 ENSRNOG00000023220

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Description

CCR4-NOT transcription complex, subunit 11 [Source:RGD Symbol;Acc:1560909]

Gene Synonyms

LOC363221, RGD1560909

Location

Primary_assembly 9: 49,309,518-49,321,771 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 1 transcript (splice variant) and 203 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000031352.7	Cnot11-201	3428	550aa	ENSRNOP00000035943.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0BNA9	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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