Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: ect2 ENSDARG00000007278

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Description

epithelial cell transforming 2 [Source:NCBI gene (formerly Entrezgene);Acc:445406]

Location

Chromosome 11: 10,388,303-10,456,553 reverse strand.

GRCz11:CM002895.2

About this gene

This gene has 5 transcripts (splice variants), 219 orthologues and is associated with 17 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000081827.4	ect2-202	4186	976aa	ENSDARP00000076266.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QVS6	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,
ENSDART00000185574.1	ect2-204	8427	980aa	ENSDARP00000144703.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8Q1Z1	-
ENSDART00000188276.1	ect2-205	8263	944aa	ENSDARP00000146880.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AB32U339	-
ENSDART00000169509.3	ect2-203	4793	1012aa	ENSDARP00000134213.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M2B2N3	-
ENSDART00000011087.6	ect2-201	3054	878aa	ENSDARP00000004102.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6DRB9	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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