Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: CNOT7 ENSDARG00000032116

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Description

CCR4-NOT transcription complex, subunit 7 [Source:ZFIN;Acc:ZDB-GENE-061013-29]

Location

Chromosome 14: 30,413,312-30,425,984 forward strand.

GRCz11:CM002898.2

About this gene

This gene has 3 transcripts (splice variants), 248 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000092953.7	CNOT7-201	2242	286aa	ENSDARP00000087385.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q08BM8	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,
ENSDART00000186864.1	CNOT7-203	4086	286aa	ENSDARP00000156128.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q08BM8	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,
ENSDART00000136009.2	CNOT7-202	2602	224aa	ENSDARP00000113903.1	Nonsense mediated decay	-	-

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Summary

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