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

Configure this page

Share this page

Bookmark this page

.

Gene: Cnot8 ENSRNOG00000002630

.

Description

CCR4-NOT transcription complex, subunit 8 [Source:RGD Symbol;Acc:1306401]

Gene Synonyms

LOC363603, MGC94581

Location

Primary_assembly 10: 42,782,283-42,795,207 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 208 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000003555.6	Cnot8-201	2466	292aa	ENSRNOP00000003555.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HEQ7 F7F1V4	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,

.

Summary

.

.