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

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Gene: E2f6 ENSRNOG00000004449

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Description

E2F transcription factor 6 [Source:RGD Symbol;Acc:631412]

Location

Primary_assembly 6: 45,320,996-45,337,428 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 2 transcripts (splice variants), 248 orthologues, 7 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000060499.6	E2f6-201	2431	272aa	ENSRNOP00000057241.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4ACR8	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,
ENSRNOT00000096820.2	E2f6-202	2498	237aa	ENSRNOP00000076801.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4ACR8	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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Paralogues

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