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: Eaf2 ENSRNOG00000002350

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Description

ELL associated factor 2 [Source:RGD Symbol;Acc:628879]

Location

Primary_assembly 11: 77,406,020-77,509,993 forward strand.

GRCr8:CM070401.1

About this gene

This gene has 3 transcripts (splice variants), 203 orthologues, 1 paralogue and is associated with 8 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000150404.1	Eaf2-203	1184	264aa	ENSRNOP00000101081.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000141098.1	Eaf2-202	1127	245aa	ENSRNOP00000105762.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000003208.7	Eaf2-201	1107	262aa	ENSRNOP00000003208.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IRB1 Q811X5	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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