Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: CNOT6L ENSPTRG00000016198

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Description

CCR4-NOT transcription complex subunit 6 like [Source:VGNC Symbol;Acc:VGNC:8261]

Location

Chromosome 4: 52,674,353-52,770,467 forward strand.

Pan_tro_3.0:CM000318.3

About this gene

This gene has 2 transcripts (splice variants), 215 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000030147.6	CNOT6L-201	1689	562aa	ENSPTRP00000027832.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XNK1 H2QPR6	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,
ENSPTRT00000083338.1	CNOT6L-202	1970	555aa	ENSPTRP00000073298.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S8J0 A0A6D2WIU3	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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